Canonical Allele Identifier: PA2826318065
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 551862
ClinVar RCV Id: RCV000667021
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Ala883Ser
CA388032190
NM_001243182.2:c.2647G>T