Canonical Allele Identifier: PA2827973409
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470153

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser278Gly
CA16023315
NM_001354899.2:c.832A>G