Canonical Allele Identifier: PA2741923475
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2963127
ClinVar RCV Id: RCV003822781
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Thr378Ser
CA2839229
NM_006005.3:c.1132A>T
CA356174321
NM_006005.3:c.1133C>G