Canonical Allele Identifier: PA2499243180
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 1163690
ClinVar RCV Id: RCV001508950

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244918.1:p.Gly423Ala
CA412196844
NM_001257989.1:c.1268G>C