Canonical Allele Identifier: PA2825038009
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1420821
ClinVar RCV Id: RCV001923592

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Thr361Ile
CA388039128
NM_000053.4:c.1082C>T