Canonical Allele Identifier: PA228962
Gene: CLCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 100781
ClinVar RCV Id: RCV000087143 RCV000520512
ClinVar Variation Id: 224917
ClinVar RCV Id: RCV000239727
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001821.2:p.Gly544Arg
CA228961
NM_001830.3:c.1630G>A
CA10576002
NM_001830.3:c.1630G>C