Canonical Allele Identifier: PA2828012485
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490366

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Phe2529Tyr
CA16038409
NM_001354902.2:c.7586T>A