Canonical Allele Identifier: PA145690
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 92389
ClinVar RCV Id: RCV000078053 RCV000490530 RCV002354273 RCV003333954
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Val1297Ile
CA145689
NM_000053.4:c.3889G>A