Canonical Allele Identifier: PA2827325241
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 312394

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Ser391Leu
CA6989425
NM_001330578.2:c.1172C>T