Canonical Allele Identifier: PA2580252678
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 2192708
ClinVar RCV Id: RCV002607613

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001944.1:p.Ser65Arg
CA10321857
NM_001953.5:c.195C>G
CA10321858
NM_001953.5:c.195C>A
CA412202496
NM_001953.5:c.193A>C