Canonical Allele Identifier: PA916028268
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 254761
ClinVar RCV Id: RCV000252230
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Ala638Thr
CA10587174
NM_001330578.2:c.1912G>A