Canonical Allele Identifier: PA2828023443
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 927485

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Gly1602Arg
CA16032494
NM_001354903.2:c.4804G>A
CA16032495
NM_001354903.2:c.4804G>C