Canonical Allele Identifier: PA2827329287
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3075464
ClinVar RCV Id: RCV004016982
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Thr810Ser
CA388034332
NM_001330579.2:c.2429C>G
CA388034335
NM_001330579.2:c.2428A>T