Canonical Allele Identifier: PA2827974832
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469744

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser759Gly
CA031761
NM_001354899.2:c.2275A>G