Canonical Allele Identifier: PA645390940
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 370887
ClinVar RCV Id: RCV000410970

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Pro768Leu
CA16041671
NM_000053.4:c.2303C>T