Canonical Allele Identifier: PA645444537
Gene: CRYGS HGNC NCBI

Linked Data

ClinVar Variation Id: 252949
ClinVar RCV Id: RCV000490776
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060011.1:p.Phe10_Tyr11delinsLeuAsn
CA16609304
NM_017541.4:c.30_31delinsAA