Canonical Allele Identifier: PA2573273902
Gene: TMEM63C HGNC NCBI

Linked Data

ClinVar Variation Id: 1686353
ClinVar RCV Id: RCV002246866
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065164.2:p.Thr115Ala
CA263807555
NM_020431.4:c.343A>G