Canonical Allele Identifier: PA2825619862
Gene: SLC25A19 HGNC NCBI
ClinVar RCV:
RCV004456430
ClinVar Variation:
3163613
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119594.1:p.Gly297Val
CA8760867
NM_001126122.2:c.890G>T