Canonical Allele Identifier: PA2828328949
Gene: CSRP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 163009

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356333.1:p.Ala90Thr
CA175600
NM_001369404.1:c.268G>A