Allele Registry

Canonical Allele Identifier: PA212267

Gene: HSPA9 HGNC NCBI

ClinVar RCV:

RCV000209966

ClinVar Variation:

224329

HGVS (amino-acid)	Matching Registered Transcripts
NP_004125.3:p.Tyr128Cys	CA212266 NM_004134.7:c.383A>G