Canonical Allele Identifier: PA346706
Gene: TMEM43 HGNC NCBI

Linked Data

ClinVar Variation Id: 180546
ClinVar RCV Id: RCV000157525 RCV002399565 RCV003600362
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077310.1:p.Phe353Leu
CA024565
NM_024334.3:c.1059C>G
CA351536457
NM_024334.3:c.1057T>C
CA351536461
NM_024334.3:c.1059C>A