Canonical Allele Identifier: PA100960
Gene: CRYGS HGNC NCBI

Linked Data

ClinVar Variation Id: 16936
ClinVar RCV Id: RCV000018444 RCV003315504
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060011.1:p.Gly18Val
CA126996
NM_017541.4:c.53G>T