Canonical Allele Identifier: PA278759
Gene: CHCHD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 218882
ClinVar RCV Id: RCV000203229 RCV003556254
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057223.1:p.Thr61Ile
CA278758
NM_016139.4:c.182C>T