Canonical Allele Identifier: PA2828054516
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469744

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser627Gly
CA031761
NM_001354905.2:c.1879A>G