Canonical Allele Identifier: PA091841
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3859

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Asn1270Ser
CA252896
NM_000053.4:c.3809A>G