Canonical Allele Identifier: PA2827329799
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_001317508.1:p.Val1022Asp
CA6988740
NM_001330579.2:c.3065T>A