Canonical Allele Identifier: PA2825024709
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482473

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser2562Gly
CA16038018
NM_000038.6:c.7684A>G