Canonical Allele Identifier: PA916028392
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 35703
ClinVar RCV Id: RCV000029352 RCV000374856 RCV000514302 RCV002390119 RCV003934854
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Val536Ala
CA260129
NM_001330579.2:c.1607T>C