Canonical Allele Identifier: PA2828328961
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_001356333.1:p.Lys113Asn
CA335112
NM_001369404.1:c.339G>T
CA5916532
NM_001369404.1:c.339G>C