Canonical Allele Identifier: PA2826560371
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 492648

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Ser306Leu
CA000994
NM_001276695.3:c.917C>T