Canonical Allele Identifier: PA916042299
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 219459

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ser990Asn
CA349100
NM_001354902.2:c.2969G>A