Canonical Allele Identifier: PA2827991993
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418008

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ala381Thr
CA16024191
NM_001354901.2:c.1141G>A