Canonical Allele Identifier: PA2826713332
Gene: CTNND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2688895
ClinVar RCV Id: RCV003490660
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001275644.1:p.Pro129Ser
CA359282149
NM_001288715.1:c.385C>T