Canonical Allele Identifier: PA2825038356
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2715663
ClinVar RCV Id: RCV003503862

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Leu709Phe
CA6989103
NM_000053.4:c.2125C>T