Canonical Allele Identifier: PA1139710676
Gene: CSRP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 944590

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003467.1:p.Ile56Met
CA5916632
NM_003476.4:c.168C>G