Canonical Allele Identifier: PA2826880568
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_001290179.1:p.Met218Ile
CA3364777
NM_001303250.3:c.654G>T
CA125344934
NM_001303250.3:c.654G>C
CA360696493
NM_001303250.3:c.654G>A