Canonical Allele Identifier: PA2827329738
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3073800
ClinVar RCV Id: RCV004016806

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Glu1002Asp
CA388028923
NM_001330579.2:c.3006G>T
CA388028926
NM_001330579.2:c.3006G>C