Canonical Allele Identifier: PA2580529274
Gene: TMEM86A HGNC NCBI

Linked Data

ClinVar Variation Id: 2259653
ClinVar RCV Id: RCV004115447
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_699178.1:p.Tyr213Cys
CA379500233
NM_153347.3:c.638A>G