Canonical Allele Identifier: PA2830435215
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 1485307
ClinVar RCV Id: RCV002030373

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_954987.2:p.Arg304Ser
CA379126529
NM_199293.3:c.910C>A