Canonical Allele Identifier: PA111694
Gene: SRP72 HGNC NCBI

Linked Data

ClinVar Variation Id: 31660

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008878.3:p.Arg207His
CA129879
NM_006947.4:c.620G>A