Canonical Allele Identifier: PA2828062491
Gene: CHM HGNC NCBI

Linked Data

ClinVar Variation Id: 3028621
ClinVar RCV Id: RCV003890486

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349447.1:p.Pro41Thr
CA413786743
NM_001362518.1:c.121C>A