Canonical Allele Identifier: PA308864
Gene: TMEM43 HGNC NCBI

Linked Data

ClinVar Variation Id: 202119
ClinVar RCV Id: RCV000183939 RCV000618132 RCV000766915 RCV000769156 RCV002485232 RCV000642423
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077310.1:p.Arg240Cys
CA024748
NM_024334.3:c.718C>T