Canonical Allele Identifier: PA2827326926
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 382098
ClinVar RCV Id: RCV000427717 RCV001828411 RCV002265761
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Thr1130Met
CA6988621
NM_001330578.2:c.3389C>T