Canonical Allele Identifier: PA2827327646
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3075569
ClinVar RCV Id: RCV004017087

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Asp1368Glu
CA388018998
NM_001330578.2:c.4104C>G
CA388018999
NM_001330578.2:c.4104C>A