Canonical Allele Identifier: PA645481073
Gene: TMEM43 HGNC NCBI

Linked Data

ClinVar Variation Id: 235059
ClinVar RCV Id: RCV000223930 RCV000243510 RCV000864384 RCV001191115 RCV001529413
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077310.1:p.Cys354Ser
CA051095
NM_024334.3:c.1061G>C
CA351536464
NM_024334.3:c.1060T>A