Canonical Allele Identifier: PA2825051946
Gene: CLCN5 HGNC NCBI

Linked Data

ClinVar Variation Id: 591443
ClinVar RCV Id: RCV000722622
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000075.1:p.Asp391Ala
CA413185937
NM_000084.5:c.1172A>C