Canonical Allele Identifier: PA1139724886
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 847832
ClinVar RCV Id: RCV001051461 RCV003326532
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Ile279Val
CA388041043
NM_001330579.2:c.835A>G