Canonical Allele Identifier: PA2741943921
Gene: TMEM63A HGNC NCBI

Linked Data

ClinVar Variation Id: 2606686
ClinVar RCV Id: RCV003354901
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055513.2:p.Ile621Phe
CA1419000
NM_014698.3:c.1861A>T