Canonical Allele Identifier: PA2827329629
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 991417
ClinVar RCV Id: RCV001279626
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Lys936Asn
CA388031699
NM_001330579.2:c.2808G>C
CA388031701
NM_001330579.2:c.2808G>T