Canonical Allele Identifier: PA2825280011
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1731793
ClinVar RCV Id: RCV002457330 RCV003099511
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Leu952Phe
CA388026461
NM_001005918.3:c.2856A>T
CA388026464
NM_001005918.3:c.2856A>C