Canonical Allele Identifier: PA2827326612
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3073800
ClinVar RCV Id: RCV004016806
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Glu1008Asp
CA388028923
NM_001330578.2:c.3024G>T
CA388028926
NM_001330578.2:c.3024G>C