Canonical Allele Identifier: PA1139746638
Gene: SLC25A46 HGNC NCBI

Linked Data

ClinVar Variation Id: 853880
ClinVar RCV Id: RCV001058788
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620128.1:p.Met309Ile
CA3364777
NM_138773.4:c.927G>T
CA125344934
NM_138773.4:c.927G>C
CA360696493
NM_138773.4:c.927G>A