Canonical Allele Identifier: PA2827329714
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3848
ClinVar RCV Id: RCV000004052 RCV000078049 RCV002321470
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.His985Gln
CA220309
NM_001330579.2:c.2955C>A
CA388029876
NM_001330579.2:c.2955C>G