Canonical Allele Identifier: PA130450
Gene: DDHD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 39679
ClinVar RCV Id: RCV000032883 RCV000449619 RCV001569601 RCV001847628
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056029.2:p.Asp660His
CA130449
NM_015214.3:c.1978G>C