Canonical Allele Identifier: PA091950
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 35706
ClinVar RCV Id: RCV000029355 RCV000078041 RCV002444440
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Met769Val
CA171300
NM_000053.4:c.2305A>G