Canonical Allele Identifier: PA2827990792
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 419952

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Glu15Ala
CA031365
NM_001354901.2:c.44A>C