Canonical Allele Identifier: PA2827325411
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 962033
ClinVar RCV Id: RCV001235818

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Ala476Val
CA388035654
NM_001330578.2:c.1427C>T