Canonical Allele Identifier: PA2825809253
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_001129496.1:p.Ser211Leu
CA207668
NM_001136024.4:c.632C>T