Canonical Allele Identifier: PA2827329271
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2505172
ClinVar RCV Id: RCV003233350

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Val806Leu
CA388034432
NM_001330579.2:c.2416G>T
CA388034434
NM_001330579.2:c.2416G>C