Canonical Allele Identifier: PA2825279952
Gene: ATP7B HGNC NCBI
ClinVar Allele:
186885
ClinVar RCV:
RCV000169142
ClinVar Variation:
188808
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Gly894Arg
CA273987
NM_001005918.3:c.2680G>A
CA388028531
NM_001005918.3:c.2680G>C