Canonical Allele Identifier: PA2825963560
Gene: TWNK HGNC NCBI

Linked Data

ClinVar Variation Id: 2034275
ClinVar RCV Id: RCV002867764

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157284.1:p.Pro70Ser
CA378206322
NM_001163812.2:c.208C>T