Canonical Allele Identifier: PA2827325222
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 663268
ClinVar RCV Id: RCV000821118
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Glu385Asp
CA388038675
NM_001330578.2:c.1155A>T
CA388038678
NM_001330578.2:c.1155A>C