Canonical Allele Identifier: PA2826754131
Gene: HELLS HGNC NCBI

Linked Data

ClinVar Variation Id: 1586082
ClinVar RCV Id: RCV002098009
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001275996.1:p.Arg53Cys
CA5615186
NM_001289067.2:c.157C>T