Canonical Allele Identifier: PA916044315
Gene: CRYAA HGNC NCBI

Linked Data

ClinVar Variation Id: 16957
ClinVar RCV Id: RCV000018469 RCV001091467
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350695.1:p.Arg79Cys
CA214969
NM_001363766.1:c.235C>T