Canonical Allele Identifier: PA091955
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 189139
ClinVar RCV Id: RCV000169558 RCV001310695
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Pro1273Leu
CA274408
NM_000053.4:c.3818C>T