Canonical Allele Identifier: PA2827325253
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 852844
ClinVar RCV Id: RCV001057545
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Leu394Phe
CA6989422
NM_001330578.2:c.1182G>C
CA388038527
NM_001330578.2:c.1182G>T