Canonical Allele Identifier: PA2827975244
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 188207
ClinVar RCV Id: RCV000168132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser878Ala
CA007751
NM_001354899.2:c.2632T>G