Canonical Allele Identifier: PA2826811787
Gene: NHS HGNC NCBI

Linked Data

ClinVar Variation Id: 129778
ClinVar RCV Id: RCV000117794 RCV002528221 RCV002390267
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278796.1:p.Leu256Val
CA231333
NM_001291867.2:c.766C>G