Canonical Allele Identifier: PA2825038505
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2572561
ClinVar RCV Id: RCV003314446

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Asn878Lys
CA388034704
NM_000053.4:c.2634T>A
CA388034710
NM_000053.4:c.2634T>G