Canonical Allele Identifier: PA2827325127
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_001317507.1:p.Gly333Glu
CA6989457
NM_001330578.2:c.998G>A
CA645573971
NM_001330578.2:c.998_999delinsAA