Canonical Allele Identifier: PA2827326048
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 558460
ClinVar RCV Id: RCV000674734

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Ala796Pro
CA250085276
NM_001330578.2:c.2386G>C