Canonical Allele Identifier: PA2826873472
Gene: CHCHD10 HGNC NCBI

Linked Data

ClinVar Variation Id: 473421
ClinVar RCV Id: RCV000558937 RCV002530220
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001288268.1:p.Ala72Thr
CA10145294
NM_001301339.2:c.214G>A