Canonical Allele Identifier: PA645436211
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376613
ClinVar RCV Id: RCV000418378 RCV000419005 RCV000419924 RCV000421156 RCV000423999 RCV000425273 RCV000425552 RCV000425919 RCV000430614 RCV000431849 RCV000429967 RCV000432462 RCV000436250 RCV000434704 RCV000436620 RCV000438391 RCV000440641 RCV000441340 RCV000442175 RCV000444718 RCV003509527 RCV004022219
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.His61Asp
CA16603034
NM_001126117.1:c.181C>G