Canonical Allele Identifier: PA2827329751
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 312382
ClinVar RCV Id: RCV000343352 RCV002261043 RCV002282117
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Thr1008Met
CA6988748
NM_001330579.2:c.3023C>T