Canonical Allele Identifier: PA2827324907
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 92390
ClinVar RCV Id: RCV000436240 RCV001001253 RCV003935015
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Ile210Val
CA220311
NM_001330578.2:c.628A>G