Canonical Allele Identifier: PA915983397
Gene: TMEM186 HGNC NCBI

Linked Data

ClinVar Variation Id: 702357
ClinVar RCV Id: RCV000871399 RCV001817006
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056236.2:p.Met1Val