Canonical Allele Identifier: PA916075706
Gene: SLC25A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 310797
ClinVar RCV Id: RCV000394919
ClinVar Variation Id: 2047772
ClinVar RCV Id: RCV002926940
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_998776.1:p.Phe2Leu
CA6732781
NM_213611.3:c.6C>G
CA10633770
NM_213611.3:c.4T>C
CA386161467
NM_213611.3:c.6C>A