Canonical Allele Identifier: PA2825037981
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2070655
ClinVar RCV Id: RCV002971317
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Gly333Glu
CA6989457
NM_000053.4:c.998G>A
CA645573971
NM_000053.4:c.998_999delinsAA