Canonical Allele Identifier: PA2826811961
Gene: NHS HGNC NCBI

Linked Data

ClinVar Variation Id: 211595
ClinVar RCV Id: RCV000193889 RCV003621519
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278797.1:p.Ser190Leu
CA207668
NM_001291868.2:c.569C>T