Canonical Allele Identifier: PA1139701120
Gene: DIAPH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 842455
ClinVar RCV Id: RCV001044881
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005210.3:p.Pro691Ser
CA361518490
NM_005219.5:c.2071C>T