Canonical Allele Identifier: PA2827326690
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 371498
ClinVar RCV Id: RCV000411980 RCV001508707
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Val1028Asp
CA6988740
NM_001330578.2:c.3083T>A