Canonical Allele Identifier: PA2573160084
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1506931
ClinVar RCV Id: RCV002007089

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Leu783Phe
CA6989056
NM_000053.4:c.2349G>C
CA388020452
NM_000053.4:c.2349G>T