Canonical Allele Identifier: PA2741900052
Gene: SOX11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2507151
ClinVar RCV Id: RCV003239042
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003099.1:p.Met27Thr
CA345865881
NM_003108.4:c.80T>C