Canonical Allele Identifier: PA274406
Gene: HEXA HGNC NCBI

Linked Data

ClinVar Variation Id: 189126
ClinVar RCV Id: RCV000169541 RCV000255876
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000511.2:p.Met1Thr