Canonical Allele Identifier: PA103473
Gene: CRYAA HGNC NCBI

Linked Data

ClinVar Variation Id: 16959
ClinVar RCV Id: RCV000018472
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000385.1:p.Arg49Cys
CA214970
NM_000394.4:c.145C>T