Canonical Allele Identifier: PA2825038645
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 991417
ClinVar RCV Id: RCV001279626
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Lys1020Asn
CA388031699
NM_000053.4:c.3060G>C
CA388031701
NM_000053.4:c.3060G>T