Canonical Allele Identifier: PA335108
Gene: CSRP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 201694
ClinVar RCV Id: RCV000320610 RCV001341005 RCV002444740 RCV001704877
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003467.1:p.Ala77Ser
CA335106
NM_003476.4:c.229G>T