Canonical Allele Identifier: PA2825280286
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 188908
ClinVar RCV Id: RCV000169268 RCV003480071
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Ser1156Phe
CA274112
NM_001005918.3:c.3467C>T