Canonical Allele Identifier: PA2825279811
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2683626
ClinVar RCV Id: RCV003480446

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Lys803Asn
CA388031895
NM_001005918.3:c.2409G>T
CA388031898
NM_001005918.3:c.2409G>C