Canonical Allele Identifier: PA2826450062
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 1426821
ClinVar RCV Id: RCV001949821
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244918.1:p.Arg303Lys
CA10321541
NM_001257989.1:c.908G>A