Canonical Allele Identifier: PA2828016447
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 926362

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Leu346Ser
CA16025442
NM_001354906.2:c.1037T>C