Canonical Allele Identifier: PA190662
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 184979
ClinVar RCV Id: RCV000164329 RCV000255425 RCV000418086 RCV000418288 RCV000428340 RCV000423280 RCV000424475 RCV000425611 RCV000434391 RCV000427767 RCV000417979 RCV000433342 RCV000423052 RCV000439433 RCV000440903 RCV000429618 RCV000445029 RCV000434549 RCV000435651 RCV000435870 RCV000439827 RCV000445148 RCV000460847 RCV000785346 RCV002288732 RCV003474857
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.His193Arg
CA000274
NM_001126112.3:c.578A>G