Canonical Allele Identifier: PA2826811877
Gene: NHS HGNC NCBI

Linked Data

ClinVar Variation Id: 198289
ClinVar RCV Id: RCV000179566 RCV000876610 RCV002317057
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278796.1:p.Ser1125Leu
CA203353
NM_001291867.2:c.3374C>T