Canonical Allele Identifier: PA2825964066
Gene: TWNK HGNC NCBI

Linked Data

ClinVar Variation Id: 2097675
ClinVar RCV Id: RCV003028517

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157286.1:p.Met32Val
CA378210947
NM_001163814.2:c.94A>G