Canonical Allele Identifier: PA2826096295
Gene: TMEM216 HGNC NCBI

Linked Data

ClinVar Variation Id: 289981
ClinVar RCV Id: RCV000291175 RCV000345935 RCV000401686 RCV001240998 RCV001788191
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001167461.1:p.Val47Ala
CA6034711
NM_001173990.3:c.140T>C