Canonical Allele Identifier: PA2827975578
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233468

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ala977Val
CA10578347
NM_001354899.2:c.2930C>T