Canonical Allele Identifier: PA2825206234
Gene: HEXA HGNC NCBI

Linked Data

ClinVar Variation Id: 811826
ClinVar RCV Id: RCV001002232 RCV001827157
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000511.2:p.Leu11Pro
CA7645127
NM_000520.6:c.32T>C