Canonical Allele Identifier: PA2825280030
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3073072
ClinVar RCV Id: RCV004015086

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Val975Leu
CA388025959
NM_001005918.3:c.2923G>T
CA388025964
NM_001005918.3:c.2923G>C