Canonical Allele Identifier: PA2827325027
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 847832

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Ile279Val
CA388041043
NM_001330578.2:c.835A>G