Canonical Allele Identifier: PA2573192958
Gene: HELLS HGNC NCBI

Linked Data

ClinVar Variation Id: 1433886
ClinVar RCV Id: RCV001984478

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276000.1:p.Asn13Ser
CA5615272
NM_001289071.2:c.38A>G