Canonical Allele Identifier: PA916019202
Gene: LYST HGNC NCBI

Linked Data

ClinVar Variation Id: 662722
ClinVar RCV Id: RCV000820438 RCV003396444
ClinVar Variation Id: 1387174
ClinVar RCV Id: RCV001905975
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001288294.1:p.Ser814Arg
CA1467276
NM_001301365.1:c.2442T>A
CA344957216
NM_001301365.1:c.2442T>G
CA344957233
NM_001301365.1:c.2440A>C