Canonical Allele Identifier: PA2830530680
Gene: CHCHD10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1963379
ClinVar RCV Id: RCV002715840
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_998885.1:p.Ser120Phe
CA410914507
NM_213720.3:c.359C>T