Canonical Allele Identifier: PA2580282322
Gene: CSRP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1699784
ClinVar RCV Id: RCV002273641 RCV003096166
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003467.1:p.His52Gln
CA218633641
NM_003476.4:c.156T>G
CA379888368
NM_003476.4:c.156T>A