Canonical Allele Identifier: PA2825207802
Gene: HEXB HGNC NCBI

Linked Data

ClinVar Variation Id: 435414
ClinVar RCV Id: RCV000500181
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000512.2:p.Tyr260His
CA360066974
NM_000521.4:c.778T>C