Canonical Allele Identifier: PA116828
Gene: CLRN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 4395
ClinVar RCV Id: RCV000004645 RCV000504948 RCV000489880 RCV000844692 RCV000999864 RCV001073333 RCV001273483 RCV001824560 RCV002504744 RCV003466812
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243748.1:p.Asn48Lys
CA116825
NM_001256819.2:c.144T>G
CA355011964
NM_001256819.2:c.144T>A