Canonical Allele Identifier: PA2825207381
Gene: HEXA HGNC NCBI

Linked Data

ClinVar Variation Id: 2150882
ClinVar RCV Id: RCV003067791 RCV003477043
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000511.2:p.Glu447Lys
CA7644713
NM_000520.6:c.1339G>A