Canonical Allele Identifier: PA184526
Gene: CSRP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 179488

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003467.1:p.Gly180Val
CA184524
NM_003476.4:c.539G>T