Canonical Allele Identifier: PA658667903
Gene: HSPB8 HGNC NCBI

Linked Data

ClinVar Variation Id: 464509
ClinVar RCV Id: RCV000538374 RCV003278890
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055180.1:p.Pro89Gln
CA6819539
NM_014365.3:c.266C>A