Canonical Allele Identifier: PA2827326605
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 495412

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Leu1005Phe
CA388029024
NM_001330578.2:c.3013C>T