Canonical Allele Identifier: PA2825154357
Gene: CHM HGNC NCBI

Linked Data

ClinVar Variation Id: 523365
ClinVar RCV Id: RCV000626681
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000381.1:p.Ala26del
CA658799817
NM_000390.4:c.75_77del