Canonical Allele Identifier: PA916047835
Gene: CSRP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 179488
ClinVar RCV Id: RCV000156278 RCV002345517 RCV003764967
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356333.1:p.Val124Leu
CA184524
NM_001369404.1:c.370G>T
CA379887529
NM_001369404.1:c.370G>C