Canonical Allele Identifier: PA2827984738
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1009641

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Asp981Gly
CA16028046
NM_001354900.2:c.2942A>G