Canonical Allele Identifier: PA1139742062
Gene: CRYAA HGNC NCBI

Linked Data

ClinVar Variation Id: 898795
ClinVar RCV Id: RCV001142886
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350695.1:p.Arg82Cys
CA321171079
NM_001363766.1:c.244C>T