Canonical Allele Identifier: PA2828004399
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1381000

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Arg2579Gly
CA16038727
NM_001354902.2:c.7735A>G