Canonical Allele Identifier: PA2573168042
Gene: CHM HGNC NCBI

Linked Data

ClinVar Variation Id: 1355379
ClinVar RCV Id: RCV001876487

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000381.1:p.Ile536Leu
CA413787481
NM_000390.4:c.1606A>C
CA413787482
NM_000390.4:c.1606A>T