Canonical Allele Identifier: PA916028399
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 385010
ClinVar RCV Id: RCV000423231 RCV001861551
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Thr587Met
CA6989232
NM_001330579.2:c.1760C>T