Canonical Allele Identifier: PA1139707569
Gene: HSPB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 948718
ClinVar RCV Id: RCV001220029
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001531.1:p.Gly84Trp
CA4306296
NM_001540.5:c.250G>T