Canonical Allele Identifier: PA2827974307
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490227

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ala576Val
CA16025286
NM_001354899.2:c.1727C>T