Canonical Allele Identifier: PA2573199315
Gene: HEXA HGNC NCBI

Linked Data

ClinVar Variation Id: 1491736
ClinVar RCV Id: RCV001988862
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305754.1:p.Gly439Asp
CA393060601
NM_001318825.2:c.1316G>A