Canonical Allele Identifier: PA1139717294
Gene: SPR HGNC NCBI

Linked Data

ClinVar Variation Id: 863750
ClinVar RCV Id: RCV001070794 RCV001195815 RCV001760052
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003115.1:p.Ser103Cys
CA1708931
NM_003124.5:c.308C>G