Canonical Allele Identifier: PA2825809549
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_001129496.1:p.Thr793Met
CA10358774
NM_001136024.4:c.2378C>T