Canonical Allele Identifier: PA103439
Gene: NSDHL HGNC NCBI

Linked Data

ClinVar Variation Id: 11430
ClinVar RCV Id: RCV000012183
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123237.1:p.Ala182Pro
CA255884
NM_001129765.2:c.544G>C