Canonical Allele Identifier: PA2827996036
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 234162

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ala1641Val
CA10578393
NM_001354901.2:c.4922C>T