Canonical Allele Identifier: PA916047837
Gene: CSRP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 163004

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356333.1:p.Arg143His
CA175595
NM_001369404.1:c.428G>A