Canonical Allele Identifier: PA2827326858
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3073072
ClinVar RCV Id: RCV004015086

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Val1104Leu
CA388025959
NM_001330578.2:c.3310G>T
CA388025964
NM_001330578.2:c.3310G>C