Canonical Allele Identifier: PA2826137290
Gene: ASNS HGNC NCBI

Linked Data

ClinVar Variation Id: 800534
ClinVar RCV Id: RCV000984516 RCV001266470 RCV001869324
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Amino-acid Alleles

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