Canonical Allele Identifier: PA2825039071
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3075569
ClinVar RCV Id: RCV004017087

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Asp1446Glu
CA388018998
NM_000053.4:c.4338C>G
CA388018999
NM_000053.4:c.4338C>A