Canonical Allele Identifier: PA271179
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 157956
ClinVar RCV Id: RCV000145281 RCV003895025
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Gly1347Ser
CA271178
NM_000053.4:c.4039G>A