Canonical Allele Identifier: PA658826466
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 554771
ClinVar RCV Id: RCV000670460 RCV001310697 RCV002469248 RCV004026114
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Thr993Met
CA6988850
NM_000053.4:c.2978C>T