Canonical Allele Identifier: PA2825279962
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 371498
ClinVar RCV Id: RCV000411980 RCV001508707
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Val899Asp
CA6988740
NM_001005918.3:c.2696T>A