Canonical Allele Identifier: PA181188
Gene: CSRP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 178014
ClinVar RCV Id: RCV000154695 RCV000764959 RCV001256872 RCV002433676
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003467.1:p.Gln91Leu
CA181186
NM_003476.4:c.272A>T