Canonical Allele Identifier: PA2827326091
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2505172
ClinVar RCV Id: RCV003233350
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Val812Leu
CA388034432
NM_001330578.2:c.2434G>T
CA388034434
NM_001330578.2:c.2434G>C