Canonical Allele Identifier: PA2826812040
Gene: NHS HGNC NCBI

Linked Data

ClinVar Variation Id: 129772
ClinVar RCV Id: RCV000117787 RCV003621503
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278797.1:p.Val485Met
CA231331
NM_001291868.2:c.1453G>A