Canonical Allele Identifier: PA2580202896
Gene: HEXA HGNC NCBI

Linked Data

ClinVar Variation Id: 2141657
ClinVar RCV Id: RCV003060421
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305754.1:p.Tyr411His
CA393061181
NM_001318825.2:c.1231T>C