Canonical Allele Identifier: PA094672
Gene: HSPB8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2617
ClinVar RCV Id: RCV000002735
ClinVar Variation Id: 2619
ClinVar RCV Id: RCV000002737 RCV000192250 RCV002472922
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055180.1:p.Lys141Asn
CA115642
NM_014365.3:c.423G>C
CA252366
NM_014365.3:c.423G>T