Canonical Allele Identifier: PA2826482801
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_001248373.1:p.Val147Ala
CA401928272
NM_001261444.2:c.440T>C