Allele Registry

Canonical Allele Identifier: PA2741921422

Gene: HSPA1L HGNC NCBI

ClinVar RCV:

RCV003979820

ClinVar Variation:

3059263

HGVS (amino-acid)	Matching Registered Transcripts
NP_005518.3:p.Glu602Lys	CA3723836 NM_005527.4:c.1804G>A