Canonical Allele Identifier: PA2830435268
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 2090085
ClinVar RCV Id: RCV003020732
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_954987.2:p.Ala328Ser
CA379126253
NM_199293.3:c.982G>T