Canonical Allele Identifier: PA2828005620
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231488

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ile1151Ser
CA10578361
NM_001354905.2:c.3452T>G