Canonical Allele Identifier: PA2825038821
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3073524
ClinVar RCV Id: RCV004016530
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Thr1178Ile
CA388026018
NM_000053.4:c.3533C>T