Canonical Allele Identifier: PA2825969104
Gene: DDHD2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157704.1:p.Gly94Trp
CA4715925
NM_001164232.2:c.280G>T