Canonical Allele Identifier: PA1139697437
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 949397
ClinVar RCV Id: RCV001220850
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Gly952Ser
CA388030552
NM_001330578.2:c.2854G>A