Canonical Allele Identifier: PA916028265
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 157930
ClinVar RCV Id: RCV000145253 RCV000415842 RCV003162602
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Gly626Ala
CA271167
NM_001330578.2:c.1877G>C