Canonical Allele Identifier: PA645440093
Gene: CRYAA HGNC NCBI

Linked Data

ClinVar Variation Id: 340099
ClinVar RCV Id: RCV000317580
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000385.1:p.Gln90Pro
CA10644750
NM_000394.4:c.269A>C