Canonical Allele Identifier: PA645436277
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376615
ClinVar RCV Id: RCV000418330 RCV000417658 RCV000422504 RCV000427653 RCV000428396 RCV000429028 RCV000429736 RCV000434864 RCV000435583 RCV000439733 RCV000445232 RCV000477234 RCV000492372 RCV001584113 RCV004022220
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.His82Arg
CA16040595
NM_001126117.1:c.245A>G