Canonical Allele Identifier: PA645466876
Gene: DHH HGNC NCBI

Linked Data

ClinVar Variation Id: 309101
ClinVar RCV Id: RCV000401936
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066382.1:p.Ala196Glu
CA6549132
NM_021044.4:c.587C>A