Canonical Allele Identifier: PA1139688343
Gene: HEXA HGNC NCBI

Linked Data

ClinVar Variation Id: 221280
ClinVar RCV Id: RCV000207246
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305754.1:p.Asp333Asn
CA074928
NM_001318825.2:c.997G>A