Canonical Allele Identifier: PA2580430432
Gene: TWNK HGNC NCBI

Linked Data

ClinVar Variation Id: 2100712
ClinVar RCV Id: RCV003014539
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068602.2:p.Trp208_Phe209insSerSerProGly
CA2580081109
NM_021830.4:c.625_626insCCTCCCCTGGGT