Canonical Allele Identifier: PA645398617
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418836

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ala15Val
CA16021438
NM_001127510.3:c.44C>T