Canonical Allele Identifier: PA2826812103
Gene: NHS HGNC NCBI

Linked Data

ClinVar Variation Id: 531901
ClinVar RCV Id: RCV000638458 RCV002438693
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278797.1:p.Thr772Met
CA10358774
NM_001291868.2:c.2315C>T