Canonical Allele Identifier: PA2825206351
Gene: HEXA HGNC NCBI

Linked Data

ClinVar Variation Id: 1465488
ClinVar RCV Id: RCV001959275
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000511.2:p.Tyr37Cys
CA393070530
NM_000520.6:c.110A>G