Canonical Allele Identifier: PA2825207147
Gene: HEXA HGNC NCBI

Linked Data

ClinVar Variation Id: 1479900
ClinVar RCV Id: RCV002009921
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000511.2:p.Gly367Ser
CA393061759
NM_000520.6:c.1099G>A