Canonical Allele Identifier: PA091880
Gene: ATP7B HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Gly1101Arg
CA273987
NM_000053.4:c.3301G>A
CA388028531
NM_000053.4:c.3301G>C