Canonical Allele Identifier: PA2827327181
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 161207
ClinVar RCV Id: RCV000148375 RCV001091634
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Asp1218Asn
CA272855
NM_001330578.2:c.3652G>A