Canonical Allele Identifier: PA915988287
Gene: CSRP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 663563
ClinVar RCV Id: RCV000821461
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003467.1:p.Cys40Tyr
CA379888440
NM_003476.4:c.119G>A