Canonical Allele Identifier: PA2827329667
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1702720
ClinVar RCV Id: RCV002279038
ClinVar Variation Id: 2124458
ClinVar RCV Id: RCV003057170

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Met956Leu
CA388030333
NM_001330579.2:c.2866A>T
CA388030341
NM_001330579.2:c.2866A>C