Canonical Allele Identifier: PA2827959823
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 423629

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Gly1777Asp
CA16032918
NM_001354897.2:c.5330G>A