Canonical Allele Identifier: PA2827962783
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1381000

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Arg2680Gly
CA16038727
NM_001354897.2:c.8038A>G