Canonical Allele Identifier: PA916018232
Gene: NHS HGNC NCBI

Linked Data

ClinVar Variation Id: 198926
ClinVar RCV Id: RCV000180386 RCV001331999
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278796.1:p.Thr1595Pro
CA247831
NM_001291867.2:c.4783A>C