Canonical Allele Identifier: PA2827330638
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 35730

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Thr1350Met
CA260152
NM_001330579.2:c.4049C>T