Canonical Allele Identifier: PA916039570
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 219535

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Val548Ala
CA028518
NM_001354896.2:c.1643T>C