Canonical Allele Identifier: PA091875
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 371021
ClinVar RCV Id: RCV000410994

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Gly1035Val
CA16041666
NM_000053.4:c.3104G>T