Canonical Allele Identifier: PA2827971918
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1381000

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Arg2645Gly
CA16038727
NM_001354898.2:c.7933A>G