Canonical Allele Identifier: PA2827978122
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141021

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Gln1736Glu
CA010025
NM_001354899.2:c.5206C>G