Canonical Allele Identifier: PA2826812131
Gene: NHS HGNC NCBI

Linked Data

ClinVar Variation Id: 198289
ClinVar RCV Id: RCV000179566 RCV000876610 RCV002317057
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278797.1:p.Ser927Leu
CA203353
NM_001291868.2:c.2780C>T