Allele Registry

Canonical Allele Identifier: PA091979

Gene: ATP7B HGNC NCBI

ClinVar RCV:

RCV000029379

RCV000224611

RCV000251030

ClinVar Variation:

35730

HGVS (amino-acid)	Matching Registered Transcripts
NP_000044.2:p.Thr1434Met	CA260152 NM_000053.4:c.4301C>T