Canonical Allele Identifier: PA2825568366
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 215343
ClinVar RCV Id: RCV000198014 RCV001833161
ClinVar Variation Id: 342149
ClinVar RCV Id: RCV000364806
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107228.1:p.Gly196Arg
CA322490
NM_001113756.3:c.586G>A
CA10321693
NM_001113756.3:c.586G>C