Canonical Allele Identifier: PA2825279836
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3075598
ClinVar RCV Id: RCV004017116
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Val817Leu
CA250080284
NM_001005918.3:c.2449G>C
CA388030741
NM_001005918.3:c.2449G>T