Canonical Allele Identifier: PA2827326918
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2097898
ClinVar RCV Id: RCV003030685
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Val1128Leu
CA388024262
NM_001330578.2:c.3382G>T
CA388024263
NM_001330578.2:c.3382G>C