Canonical Allele Identifier: PA091946
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3862

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Met645Arg
CA252899
NM_000053.4:c.1934T>G