Canonical Allele Identifier: PA2826456338
Gene: SP6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1712318
ClinVar RCV Id: RCV003329443
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245177.1:p.Ala273Lys
CA2573332356
NM_001258248.2:c.817_818delinsAA