Canonical Allele Identifier: PA2826560697
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2121740
ClinVar RCV Id: RCV003043347
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Val83Leu
CA397844318
NM_001276696.3:c.247G>T
CA397844319
NM_001276696.3:c.247G>C