Allele Registry

Canonical Allele Identifier: PA2827649689

Gene: ASNS HGNC NCBI

ClinVar RCV:

RCV000984516

RCV001266470

RCV001869324

ClinVar Variation:

800534

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339425.1:p.Arg550His	CA4354461 NM_001352496.2:c.1649G>A