Canonical Allele Identifier: PA645420986
Gene: SPR HGNC NCBI

Linked Data

ClinVar Variation Id: 336991

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003115.1:p.Asn127Ser
CA1708946
NM_003124.5:c.380A>G