Canonical Allele Identifier: PA2828050732
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 427929

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Gly49Glu
CA16022027
NM_001354905.2:c.146G>A