Canonical Allele Identifier: PA2827329023
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 590805
ClinVar RCV Id: RCV000721965

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Ala700Val
CA388020448
NM_001330579.2:c.2099C>T