Canonical Allele Identifier: PA2825038851
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2097898
ClinVar RCV Id: RCV003030685
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Val1206Leu
CA388024262
NM_000053.4:c.3616G>T
CA388024263
NM_000053.4:c.3616G>C