Canonical Allele Identifier: PA916028273
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3862
ClinVar RCV Id: RCV000004066 RCV001508347 RCV002408449 RCV003398442
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Met645Arg
CA252899
NM_001330578.2:c.1934T>G