Canonical Allele Identifier: PA2826318333
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3073072
ClinVar RCV Id: RCV004015086
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Val1071Leu
CA388025959
NM_001243182.2:c.3211G>T
CA388025964
NM_001243182.2:c.3211G>C