Canonical Allele Identifier: PA2828051895
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 822775

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser236Ile
CA051048
NM_001354905.2:c.707G>T