Canonical Allele Identifier: PA2580540533
Gene: GNAL HGNC NCBI

Linked Data

ClinVar Variation Id: 2138128
ClinVar RCV Id: RCV003064500
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_892023.1:p.Val431Ala
CA401928272
NM_182978.4:c.1292T>C