Canonical Allele Identifier: PA2827329912
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1731793

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Leu1075Phe
CA388026461
NM_001330579.2:c.3225A>T
CA388026464
NM_001330579.2:c.3225A>C