Canonical Allele Identifier: PA2499234737
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1134697
ClinVar RCV Id: RCV001469712 RCV001579789 RCV001820163
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Ala932Gly
CA6988690
NM_001005918.3:c.2795C>G