Canonical Allele Identifier: PA2827999232
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1381000

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Arg2611Gly
CA16038727
NM_001354901.2:c.7831A>G