Canonical Allele Identifier: PA658655079
Gene: TMEM199 HGNC NCBI

Linked Data

ClinVar Variation Id: 445808
ClinVar RCV Id: RCV000514416
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689677.1:p.Tyr86His
CA8457014
NM_152464.3:c.256T>C