Canonical Allele Identifier: PA2499249706
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1127570
ClinVar RCV Id: RCV001460044
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Asn637Ser
CA6989178
NM_001330578.2:c.1910A>G