Canonical Allele Identifier: PA2827980795
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 647034
ClinVar RCV Id: RCV003653346

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2553Gly
CA16038141
NM_001354899.2:c.7657A>G