Canonical Allele Identifier: PA645391081
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 381534
ClinVar RCV Id: RCV000434557 RCV000780936
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Arg969Trp
CA6988868
NM_000053.4:c.2905C>T