Canonical Allele Identifier: PA2827327395
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 157957
ClinVar RCV Id: RCV000309770 RCV000587055 RCV000763902 RCV002252001 RCV002326851
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Pro1301Ser
CA271180
NM_001330578.2:c.3901C>T