Canonical Allele Identifier: PA2827977896
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 234162

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ala1672Val
CA10578393
NM_001354899.2:c.5015C>T