Canonical Allele Identifier: PA2827330270
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_001317508.1:p.Asp1212Asn
CA272855
NM_001330579.2:c.3634G>A