Canonical Allele Identifier: PA1139710664
Gene: CSRP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 835944
ClinVar RCV Id: RCV001036949
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003467.1:p.Ala43Ser
CA379888418
NM_003476.4:c.127G>T