Canonical Allele Identifier: PA2825154548
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_000381.1:p.Thr207Ala
CA10465556
NM_000390.4:c.619A>G