Canonical Allele Identifier: PA091813
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 188781
ClinVar RCV Id: RCV000169109 RCV001508716 RCV001814079
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Ala1003Val
CA273949
NM_000053.4:c.3008C>T