Canonical Allele Identifier: PA2580127578
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2097898
ClinVar RCV Id: RCV003030685

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Val999Leu
CA388024262
NM_001005918.3:c.2995G>T
CA388024263
NM_001005918.3:c.2995G>C