Canonical Allele Identifier: PA2825644865
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1381000

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Arg2652Gly
CA16038727
NM_001127511.3:c.7954A>G