Canonical Allele Identifier: PA2828062122
Gene: CHM HGNC NCBI

Linked Data

ClinVar Variation Id: 1106860
ClinVar RCV Id: RCV001431718
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349446.1:p.Val21Ile
CA10465567
NM_001362517.1:c.61G>A