Canonical Allele Identifier: PA2825809287
Gene: NHS HGNC NCBI

Linked Data

ClinVar Variation Id: 198291
ClinVar RCV Id: RCV000179568 RCV002444719 RCV003509508
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129496.1:p.Gly266Arg
CA246847
NM_001136024.4:c.796G>A
CA412350911
NM_001136024.4:c.796G>C