Canonical Allele Identifier: PA2827940380
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 822775

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Ser295Ile
CA051048
NM_001354895.2:c.884G>T