Canonical Allele Identifier: PA302242
Gene: SNTA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 190903
ClinVar RCV Id: RCV000171086 RCV000342871 RCV000285552 RCV001094618 RCV003165349
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003089.1:p.Ser43Asn
CA302240
NM_003098.3:c.128G>A