Canonical Allele Identifier: PA152566
Gene: DDHD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 128893
ClinVar RCV Id: RCV000116873 RCV001725969 RCV001847679 RCV001519818
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056029.2:p.Thr186Met
CA152565
NM_015214.3:c.557C>T