Canonical Allele Identifier: PA113436
Gene: TMEM43 HGNC NCBI

Linked Data

ClinVar Variation Id: 734
ClinVar RCV Id: RCV000000770 RCV000039375 RCV000183944 RCV000588763 RCV000621202 RCV001254741 RCV001181315 RCV001375655
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077310.1:p.Ser358Leu
CA024568
NM_024334.3:c.1073C>T