Canonical Allele Identifier: PA2827993813
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1009641

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Asp963Gly
CA16028046
NM_001354901.2:c.2888A>G