Canonical Allele Identifier: PA2825598742
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2087249
ClinVar RCV Id: RCV003017803
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Met44Leu
CA397846872
NM_001126112.3:c.130A>T
CA397846886
NM_001126112.3:c.130A>C