Canonical Allele Identifier: PA2580258184
Gene: CTSC HGNC NCBI

Linked Data

ClinVar Variation Id: 2105562
ClinVar RCV Id: RCV003014957
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001805.4:p.Ser342Ala
CA382022043
NM_001814.6:c.1024T>G