Canonical Allele Identifier: PA645385652
Gene: CLCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 209116
ClinVar RCV Id: RCV000239734 RCV000721130 RCV000816910 RCV002252041
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001821.2:p.Arg718Trp
CA10575780
NM_001830.3:c.2152C>T