Canonical Allele Identifier: PA2827314217
Gene: HELZ HGNC NCBI

Linked Data

ClinVar Variation Id: 3105107
ClinVar RCV Id: RCV004403948
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317376.2:p.Tyr1099His
CA400711196
NM_001330447.2:c.3295T>C