Canonical Allele Identifier: PA2827990169
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1381000

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Arg2629Gly
CA16038727
NM_001354900.2:c.7885A>G