Allele Registry

Canonical Allele Identifier: PA102997

Gene: SLC25A20 HGNC NCBI

ClinVar RCV:

RCV000012921

RCV000153966

ClinVar Variation:

12138

HGVS (amino-acid)	Matching Registered Transcripts
NP_000378.1:p.Gln238Arg	CA121918 NM_000387.6:c.713A>G