Canonical Allele Identifier: PA106862
Gene: DDHD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 39679
ClinVar RCV Id: RCV000032883 RCV000449619 RCV001569601 RCV001847628
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157704.1:p.Asp660His
CA130449
NM_001164232.2:c.1978G>C