Canonical Allele Identifier: PA2825279709
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3075464
ClinVar RCV Id: RCV004016982
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Thr732Ser
CA388034332
NM_001005918.3:c.2195C>G
CA388034335
NM_001005918.3:c.2194A>T