Canonical Allele Identifier: PA915953918
Gene: CLCN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 569127
ClinVar RCV Id: RCV000689675
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000074.3:p.Asn908Asp
CA4537773
NM_000083.3:c.2722A>G