Allele Registry

Canonical Allele Identifier: PA2826173125

Gene: HSPA12B HGNC NCBI

ClinVar RCV:

RCV000888263

ClinVar Variation:

715749

HGVS (amino-acid)	Matching Registered Transcripts
NP_001184256.1:p.Val23Leu	CA9747615 NM_001197327.2:c.67G>C CA408132037 NM_001197327.2:c.67G>T