Canonical Allele Identifier: PA2825207228
Gene: HEXA HGNC NCBI

Linked Data

ClinVar Variation Id: 2045477
ClinVar RCV Id: RCV002900532
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000511.2:p.Pro397Thr
CA7644761
NM_000520.6:c.1189C>A