Canonical Allele Identifier: PA175602
Gene: CSRP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 163009

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003467.1:p.Arg146His
CA175600
NM_003476.4:c.437G>A