ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2825568000
Gene: TYMP
HGNC
NCBI
Linked Data
ClinVar Variation Id:
223051
ClinVar RCV Id:
RCV000208689
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001107227.1:p.Leu356Pro
CA16616793
NM_001113755.3:c.1067T>C