Canonical Allele Identifier: PA658813708
Gene: TIMM8A HGNC NCBI

Linked Data

ClinVar Variation Id: 505064
ClinVar RCV Id: RCV000603847
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004076.1:p.Ser94Arg
CA413912548
NM_004085.4:c.282C>G
CA413912554
NM_004085.4:c.282C>A
CA413912587
NM_004085.4:c.280A>C