Canonical Allele Identifier: PA2829781851
Gene: HELZ HGNC NCBI

Linked Data

ClinVar Variation Id: 402158
ClinVar RCV Id: RCV000454348

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055692.3:p.Ile1108Val
CA16609539
NM_014877.4:c.3322A>G