Canonical Allele Identifier: PA2827329103
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2774738
ClinVar RCV Id: RCV003504084

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Val741Met
CA388016853
NM_001330579.2:c.2221G>A