Canonical Allele Identifier: PA2828029651
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2677462

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Val2558Leu
CA16038652
NM_001354903.2:c.7672G>C
CA16038653
NM_001354903.2:c.7672G>T