Canonical Allele Identifier: PA211238
Gene: CSRP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 8779
ClinVar RCV Id: RCV000009324
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003467.1:p.Ser54_Glu55delinsArgGly
CA211236
NM_003476.4:c.160_164delinsAGGGG