Canonical Allele Identifier: PA2580294921
Gene: SLC25A12 HGNC NCBI

Linked Data

ClinVar Variation Id: 2146551
ClinVar RCV Id: RCV003067190
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003696.2:p.Phe91Val
CA349632349
NM_003705.5:c.271T>G