Canonical Allele Identifier: PA2499227105
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1172922
ClinVar RCV Id: RCV001527078
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Trp779Cys
CA388020479
NM_000053.4:c.2337G>T
CA388020480
NM_000053.4:c.2337G>C