Canonical Allele Identifier: PA916062568
Gene: TH HGNC NCBI

Linked Data

ClinVar Variation Id: 695326
ClinVar RCV Id: RCV001103468 RCV001585801 RCV003928326
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_954987.2:p.Glu27Asp
CA5818870
NM_199293.3:c.81G>T
CA379112773
NM_199293.3:c.81G>C