Canonical Allele Identifier: PA335114
Gene: CSRP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 201696
ClinVar RCV Id: RCV000183340
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003467.1:p.Val170Phe
CA335112
NM_003476.4:c.508G>T