Canonical Allele Identifier: PA916028300
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 371021
ClinVar RCV Id: RCV000410994
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Gly957Val
CA16041666
NM_001330578.2:c.2870G>T