Canonical Allele Identifier: PA1139733696
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 371913
ClinVar RCV Id: RCV000411411

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Gly42Ser
CA16042080
NM_001354902.2:c.124G>A