Canonical Allele Identifier: PA916028291
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 555818
ClinVar RCV Id: RCV000671715
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Met939Ile
CA6988831
NM_001330578.2:c.2817G>A
CA388031765
NM_001330578.2:c.2817G>T
CA388031766
NM_001330578.2:c.2817G>C