Canonical Allele Identifier: PA645421993
Gene: SLC25A12 HGNC NCBI

Linked Data

ClinVar Variation Id: 406561
ClinVar RCV Id: RCV000456601
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003696.2:p.Phe564Leu
CA16610274
NM_003705.5:c.1692C>A
CA349287837
NM_003705.5:c.1692C>G
CA349287848
NM_003705.5:c.1690T>C