Canonical Allele Identifier: PA2825279662
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3074623
ClinVar RCV Id: RCV004014157

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Pro701Arg
CA388015300
NM_001005918.3:c.2102C>G