Allele Registry

Canonical Allele Identifier: PA915998912

Gene: HSPA1L HGNC NCBI

ClinVar RCV:

RCV000856580

ClinVar Variation:

694520

HGVS (amino-acid)	Matching Registered Transcripts
NP_005518.3:p.Thr493Lys	CA363376871 NM_005527.4:c.1478C>A