ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA645407304
Gene: TYMP
HGNC
NCBI
Linked Data
ClinVar Variation Id:
223053
ClinVar RCV Id:
RCV000208644
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001944.1:p.Gly387Ser
CA16616795
NM_001953.5:c.1159G>A