Canonical Allele Identifier: PA2825038520
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3075464
ClinVar RCV Id: RCV004016982

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Thr894Ser
CA388034332
NM_000053.4:c.2681C>G
CA388034335
NM_000053.4:c.2680A>T