Canonical Allele Identifier: PA916012698
Gene: ATP7A HGNC NCBI

Linked Data

ClinVar Variation Id: 660917

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269153.1:p.Val711Ile
CA10459200
NM_001282224.2:c.2131G>A