Allele Registry

Canonical Allele Identifier: PA2826137657

Gene: ASNS HGNC NCBI

ClinVar RCV:

RCV000984516

RCV001266470

RCV001869324

ClinVar Variation:

800534

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171547.1:p.Arg467His	CA4354461 NM_001178076.2:c.1400G>A