Canonical Allele Identifier: PA2827061834
Gene: CHM HGNC NCBI

Linked Data

ClinVar Variation Id: 39809
ClinVar RCV Id: RCV000033030
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307888.1:p.His359Arg
CA261228
NM_001320959.1:c.1076A>G