Canonical Allele Identifier: PA2827327292
Gene: ATP7B HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Gly1263Ser
CA271177
NM_001330578.2:c.3787G>A