Allele Registry

Canonical Allele Identifier: PA645476850

Gene: CSRP3 HGNC NCBI

ClinVar Variation Id: 423356

HGVS (amino-acid)	Matching Registered Transcripts
NP_003467.1:p.Lys59Glu	CA5916630 NM_003476.4:c.175A>G