Canonical Allele Identifier: PA2825025138
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1381000

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Arg2670Gly
CA16038727
NM_000038.6:c.8008A>G