Canonical Allele Identifier: PA091818
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 157952

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Ala1183Gly
CA171321
NM_000053.4:c.3548C>G