Canonical Allele Identifier: PA645407158
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 342153
ClinVar RCV Id: RCV000324061

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001944.1:p.Lys115Arg
CA10321791
NM_001953.5:c.344A>G