Canonical Allele Identifier: PA2830024267
Gene: TMEM43 HGNC NCBI

Linked Data

ClinVar Variation Id: 1765714
ClinVar RCV Id: RCV002378582
ClinVar Variation Id: 1765740

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077310.1:p.Ser303Asn
CA69733935
NM_024334.3:c.908G>A
CA2580068488
NM_024334.3:c.908_909delinsAT