Canonical Allele Identifier: PA2580304831
Gene: LY86 HGNC NCBI

Linked Data

ClinVar Variation Id: 2306068
ClinVar RCV Id: RCV004149196
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004262.1:p.Gly3Cys
CA362742562
NM_004271.4:c.7G>T