ClinGen Allele Registry
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Canonical Allele Identifier:
PA312981
Gene: SLC25A15
HGNC
NCBI
Linked Data
ClinVar Variation Id:
203939
ClinVar RCV Id:
RCV000401214
RCV000726011
RCV001251645
RCV003907650
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_055067.1:p.Arg61His
CA312980
NM_014252.4:c.182G>A