Canonical Allele Identifier: PA2499234737
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1134697

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Ala932Gly
CA6988690
NM_001005918.3:c.2795C>G