Canonical Allele Identifier: PA645466877
Gene: DHH HGNC NCBI

Linked Data

ClinVar Variation Id: 309099
ClinVar RCV Id: RCV000301984 RCV001508336
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066382.1:p.Arg309Leu
CA10641526
NM_021044.4:c.926G>T