Canonical Allele Identifier: PA2828002945
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41532

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asn1707Asp
CA010373
NM_001354902.2:c.5119A>G