Canonical Allele Identifier: PA916042269
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470153

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ser316Gly
CA16023315
NM_001354902.2:c.946A>G