Canonical Allele Identifier: PA916040040
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 568446

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Gly990Ser
CA033918
NM_001354896.2:c.2968G>A