Canonical Allele Identifier: PA2827061627
Gene: CHM HGNC NCBI

Linked Data

ClinVar Variation Id: 796016
ClinVar RCV Id: RCV000979375 RCV001832267
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307888.1:p.Thr59Ala
CA10465556
NM_001320959.1:c.175A>G