Canonical Allele Identifier: PA092121
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 188859
ClinVar RCV Id: RCV000169211 RCV000725176
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Val1216Met
CA274052
NM_000053.4:c.3646G>A