Canonical Allele Identifier: PA2827329959
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3073072
ClinVar RCV Id: RCV004015086
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Val1098Leu
CA388025959
NM_001330579.2:c.3292G>T
CA388025964
NM_001330579.2:c.3292G>C