Canonical Allele Identifier: PA2827328712
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2141850

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Ala576Val
CA6989239
NM_001330579.2:c.1727C>T