Canonical Allele Identifier: PA2573082534
Gene: SPR HGNC NCBI

Linked Data

ClinVar Variation Id: 1317114
ClinVar RCV Id: RCV001758986 RCV001868702
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003115.1:p.Val256Met
CA1709031
NM_003124.5:c.766G>A