Canonical Allele Identifier: PA353422
Gene: HSPA9 HGNC NCBI

Linked Data

ClinVar Variation Id: 224070
ClinVar RCV Id: RCV000209862

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004125.3:p.Ile458_Asn459del
CA353421
NM_004134.7:c.1373_1378del