Canonical Allele Identifier: PA2825038612
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2107627
ClinVar RCV Id: RCV003045696

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Gly1000Val
CA388032072
NM_000053.4:c.2999G>T