Canonical Allele Identifier: PA2825014100
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 822775

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser295Ile
CA051048
NM_000038.6:c.884G>T