Canonical Allele Identifier: PA067669
Gene: SLC25A42 HGNC NCBI

Linked Data

ClinVar Variation Id: 219191
ClinVar RCV Id: RCV000203566 RCV000412490 RCV000984915
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_848621.2:p.Asn291Asp
CA279953
NM_178526.5:c.871A>G