Canonical Allele Identifier: PA2825568638
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 1163690
ClinVar RCV Id: RCV001508950
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107228.1:p.Gly418Ala
CA412196844
NM_001113756.3:c.1253G>C