Canonical Allele Identifier: PA339801
Gene: TMEM216 HGNC NCBI

Linked Data

ClinVar Variation Id: 197
ClinVar RCV Id: RCV000000220 RCV000255378 RCV000409114 RCV000465185 RCV000624413 RCV000779066 RCV001787358
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057583.2:p.Arg12Leu
CA339800
NM_016499.6:c.35G>T