Canonical Allele Identifier: PA2827326339
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 35712
ClinVar RCV Id: RCV000029361 RCV000505878 RCV000255583 RCV002513236 RCV003904863
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Thr913Met
CA090896
NM_001330578.2:c.2738C>T