Canonical Allele Identifier: PA2827984696
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1063950

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ala970Val
CA16027966
NM_001354900.2:c.2909C>T