Canonical Allele Identifier: PA2827993788
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482459

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Asp957Val
CA16028005
NM_001354901.2:c.2870A>T