Canonical Allele Identifier: PA2828328972
Gene: CSRP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 303951

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356333.1:p.Arg123Gln
CA10630532
NM_001369404.1:c.368G>A