Canonical Allele Identifier: PA645391324
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 382098

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Thr1208Met
CA6988621
NM_000053.4:c.3623C>T