Canonical Allele Identifier: PA2580286193
Gene: SPR HGNC NCBI

Linked Data

ClinVar Variation Id: 2419965
ClinVar RCV Id: RCV003118490
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003115.1:p.Thr13Ile
CA347230399
NM_003124.5:c.38C>T