Canonical Allele Identifier: PA2827983669
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216153

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ala656Val
CA030702
NM_001354900.2:c.1967C>T