Canonical Allele Identifier: PA2826755098
Gene: HELLS HGNC NCBI

Linked Data

ClinVar Variation Id: 1433886
ClinVar RCV Id: RCV001984478
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276001.1:p.Asn137Ser
CA5615272
NM_001289072.2:c.410A>G