Canonical Allele Identifier: PA346702
Gene: TMEM43 HGNC NCBI

Linked Data

ClinVar Variation Id: 180544
ClinVar RCV Id: RCV000157523 RCV000467886 RCV000523010 RCV002408708 RCV002492613
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077310.1:p.Arg266Trp
CA024757
NM_024334.3:c.796C>T