Canonical Allele Identifier: PA2827061624
Gene: CHM HGNC NCBI

Linked Data

ClinVar Variation Id: 1971865
ClinVar RCV Id: RCV002745760
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307888.1:p.Glu50Gly
CA10465558
NM_001320959.1:c.149A>G