Canonical Allele Identifier: PA2825616472
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 492648
ClinVar RCV Id: RCV000582476 RCV000608773
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Ser213Leu
CA000994
NM_001126117.1:c.638C>T