Canonical Allele Identifier: PA1139724956
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 968172
ClinVar RCV Id: RCV001243246
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Ser376Phe
CA6989436
NM_001330579.2:c.1127C>T