Canonical Allele Identifier: PA2825568197
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 2415332
ClinVar RCV Id: RCV003110751
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107228.1:p.Gly20Arg
CA10321887
NM_001113756.3:c.58G>A
CA412203012
NM_001113756.3:c.58G>C