Canonical Allele Identifier: PA2827293475
Gene: TMEM216 HGNC NCBI

Linked Data

ClinVar Variation Id: 196320
ClinVar RCV Id: RCV000177125 RCV000533045 RCV001279272
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317214.1:p.Val10Leu
CA202293
NM_001330285.2:c.28G>T
CA380685167
NM_001330285.2:c.28G>C