Canonical Allele Identifier: PA2825038126
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 962033
ClinVar RCV Id: RCV001235818

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Ala476Val
CA388035654
NM_000053.4:c.1427C>T