Canonical Allele Identifier: PA2826567225
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376693
ClinVar RCV Id: RCV000423298 RCV000428749 RCV000429935 RCV000437595 RCV000440629 RCV000444464 RCV000785279 RCV001201781 RCV001559774 RCV002365462 RCV000419208 RCV000420300 RCV000425130 RCV000430980 RCV000438183 RCV004022256
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Tyr197Cys
CA16603106
NM_001276761.3:c.590A>G