Canonical Allele Identifier: PA2827984681
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233468

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ala964Val
CA10578347
NM_001354900.2:c.2891C>T