Canonical Allele Identifier: PA2828023145
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1745286

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Asp1415Val
CA16032466
NM_001354906.2:c.4244A>T