Canonical Allele Identifier: PA1139747054
Gene: TMEM43 HGNC NCBI

Linked Data

ClinVar Variation Id: 937703
ClinVar RCV Id: RCV001206778 RCV001823765
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077310.1:p.Pro386Ser
CA351536638
NM_024334.3:c.1156C>T