Canonical Allele Identifier: PA2826888327
Gene: TMEM143 HGNC NCBI
ClinVar RCV:
RCV004475186
ClinVar Variation:
3178814
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001290468.1:p.His308Arg
CA9549371
NM_001303539.2:c.923A>G