Canonical Allele Identifier: PA2825279279
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 861481
ClinVar RCV Id: RCV001068015 RCV003898074
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Met368Ile
CA388039004
NM_001005918.3:c.1104G>T
CA388039006
NM_001005918.3:c.1104G>C
CA388039010
NM_001005918.3:c.1104G>A