Canonical Allele Identifier: PA2828023219
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 825464

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser1424Phe
CA16032523
NM_001354906.2:c.4271C>T