Canonical Allele Identifier: PA2825157176
Gene: CRYAA HGNC NCBI

Linked Data

ClinVar Variation Id: 898795
ClinVar RCV Id: RCV001142886

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000385.1:p.Arg119Cys
CA321171079
NM_000394.4:c.355C>T