Canonical Allele Identifier: PA2499252146
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1059095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asp2537Gly
CA16037756
NM_001354896.2:c.7610A>G