Canonical Allele Identifier: PA2826503952
Gene: SRP72 HGNC NCBI

Linked Data

ClinVar Variation Id: 31660

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254651.1:p.Arg207His
CA129879
NM_001267722.2:c.620G>A