Canonical Allele Identifier: PA2827061784
Gene: CHM HGNC NCBI

Linked Data

ClinVar Variation Id: 2138623
ClinVar RCV Id: RCV003064744
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307888.1:p.Met295Val
CA413789619
NM_001320959.1:c.883A>G