Canonical Allele Identifier: PA096761
Gene: HSPB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 7482
ClinVar RCV Id: RCV000007910
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001531.1:p.Arg136Trp
CA254190
NM_001540.5:c.406C>T