Canonical Allele Identifier: PA658809829
Gene: CSRP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 543038

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003467.1:p.Asn158Asp
CA379887685
NM_003476.4:c.472A>G