Canonical Allele Identifier: PA2827980214
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181817
ClinVar RCV Id: RCV000159569

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asn2377Ser
CA012942
NM_001354899.2:c.7130A>G