Canonical Allele Identifier: PA137766
Gene: TMEM43 HGNC NCBI

Linked Data

ClinVar Variation Id: 46155
ClinVar RCV Id: RCV000039395 RCV000457565 RCV000766918 RCV000776154 RCV002496628 RCV003372610
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077310.1:p.Trp316Ser
CA024803
NM_024334.3:c.947G>C