Canonical Allele Identifier: PA2827061596
Gene: CHM HGNC NCBI

Linked Data

ClinVar Variation Id: 1158381

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307888.1:p.Asp14Asn
CA10465571
NM_001320959.1:c.40G>A