Canonical Allele Identifier: PA916042499
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 629986
ClinVar RCV Id: RCV000774851

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Asp974Gly
CA16028788
NM_001354905.2:c.2921A>G