Canonical Allele Identifier: PA2827329093
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1456056
ClinVar RCV Id: RCV001950954
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Arg732Ser
CA388017173
NM_001330579.2:c.2196G>T
CA388017176
NM_001330579.2:c.2196G>C