Canonical Allele Identifier: PA1139697432
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 991417
ClinVar RCV Id: RCV001279626

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Lys942Asn
CA388031699
NM_001330578.2:c.2826G>C
CA388031701
NM_001330578.2:c.2826G>T