Canonical Allele Identifier: PA2827949580
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470153

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser306Gly
CA16023315
NM_001354896.2:c.916A>G