Canonical Allele Identifier: PA2825616737
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2168377
ClinVar RCV Id: RCV003082531
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Val34Ala
CA397845710
NM_001126118.1:c.101T>C