Allele Registry

Canonical Allele Identifier: PA2826137290

Gene: ASNS HGNC NCBI

ClinVar RCV:

RCV000984516

RCV001266470

RCV001869324

ClinVar Variation:

800534

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171546.1:p.Arg529His	CA4354461 NM_001178075.2:c.1586G>A