Canonical Allele Identifier: PA916015272
Gene: CLCN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 772363
ClinVar RCV Id: RCV000951898 RCV003169468 RCV002489306
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004357.3:p.Pro381Ala
CA2734222
NM_004366.6:c.1141C>G