Canonical Allele Identifier: PA2828007786
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1059798

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Gln1592Glu
CA16032822
NM_001354905.2:c.4774C>G