Canonical Allele Identifier: PA2827991871
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233745

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Arg343Cys
CA10578309
NM_001354901.2:c.1027C>T