Canonical Allele Identifier: PA2580282320
Gene: CSRP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2056363
ClinVar RCV Id: RCV002947483
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003467.1:p.His52Pro
CA379888370
NM_003476.4:c.155A>C