Canonical Allele Identifier: PA2827325168
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2883196
ClinVar RCV Id: RCV003610716
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Gln355His
CA388039231
NM_001330578.2:c.1065G>T
CA388039232
NM_001330578.2:c.1065G>C