Canonical Allele Identifier: PA2826603194
Gene: STT3A HGNC NCBI

Linked Data

ClinVar Variation Id: 102443
ClinVar RCV Id: RCV000088679 RCV003556159
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265433.1:p.Val534Ala
CA249894
NM_001278504.2:c.1601T>C