Canonical Allele Identifier: PA091965
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 188908

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Ser1363Phe
CA274112
NM_000053.4:c.4088C>T