Canonical Allele Identifier: PA2827954339
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 371861

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Gly42Asp
CA16042081
NM_001354897.2:c.125G>A