Canonical Allele Identifier: PA2827326803
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1731793
ClinVar RCV Id: RCV002457330 RCV003099511
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Leu1081Phe
CA388026461
NM_001330578.2:c.3243A>T
CA388026464
NM_001330578.2:c.3243A>C