Canonical Allele Identifier: PA116822
Gene: CLRN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 4393
ClinVar RCV Id: RCV000004643 RCV001851649
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243748.1:p.His177Gln
CA116819
NM_001256819.2:c.531T>A
CA354955548
NM_001256819.2:c.531T>G