Canonical Allele Identifier: PA2828011058
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142044

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Met2122Val
CA012319
NM_001354902.2:c.6364A>G