Canonical Allele Identifier: PA2825568308
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 2418704
ClinVar RCV Id: RCV003121453

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107228.1:p.Lys124Asn
CA412201987
NM_001113756.3:c.372G>T
CA412201988
NM_001113756.3:c.372G>C