Canonical Allele Identifier: PA2828007480
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 438873

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Tyr936Asp
CA16028076
NM_001354902.2:c.2806T>G