Canonical Allele Identifier: PA1139740415
Gene: CHM HGNC NCBI

Linked Data

ClinVar Variation Id: 936538
ClinVar RCV Id: RCV001205355
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349448.1:p.Thr7Lys
CA413787120
NM_001362519.1:c.20C>A