ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA1139749660
Gene: CTSC
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV001041477
RCV004031252
ClinVar Variation:
839668
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_680475.1:p.Leu68Arg
CA225446938
NM_148170.5:c.203T>G