Canonical Allele Identifier: PA916012684
Gene: ATP7A HGNC NCBI

Linked Data

ClinVar Variation Id: 210410
ClinVar RCV Id: RCV000193497
ClinVar Variation Id: 210411

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269153.1:p.Gly666Arg
CA277154
NM_001282224.2:c.1996G>A
CA277408
NM_001282224.2:c.1996G>C