Canonical Allele Identifier: PA2828026830
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411434

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Arg2127Gly
CA16035939
NM_001354903.2:c.6379A>G