Canonical Allele Identifier: PA2826482768
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_001248372.1:p.Val354Ala
CA401928272
NM_001261443.2:c.1061T>C