Canonical Allele Identifier: PA2828000981
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411558

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Arg714Gln
CA031897
NM_001354902.2:c.2141G>A