Canonical Allele Identifier: PA2827987201
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141021

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Gln1723Glu
CA010025
NM_001354900.2:c.5167C>G