Canonical Allele Identifier: PA2825157977
Gene: CTSK HGNC NCBI

Linked Data

ClinVar Variation Id: 8420
ClinVar RCV Id: RCV000008931
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000387.1:p.Met329_Ter330insTrpLeuGlnProAlaLysSerIleLeuLeuPheHisPhePheHisAspGlyAlaVal
CA119606
NM_000396.4:c.990A>G