Canonical Allele Identifier: PA2827975607
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 970107
ClinVar RCV Id: RCV003652102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asp987Gly
CA16027996
NM_001354899.2:c.2960A>G