Canonical Allele Identifier: PA214999
Gene: CRYAA HGNC NCBI

Linked Data

ClinVar Variation Id: 68461
ClinVar RCV Id: RCV000059330
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000385.1:p.Arg21Gln
CA214998
NM_000394.4:c.62G>A