Canonical Allele Identifier: PA2827327307
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_001317507.1:p.Gly1269Ser
CA271178
NM_001330578.2:c.3805G>A