Canonical Allele Identifier: PA2828022165
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2444634
ClinVar RCV Id: RCV003154402

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Gly1251Arg
CA16031406
NM_001354906.2:c.3751G>A
CA16031407
NM_001354906.2:c.3751G>C