Canonical Allele Identifier: PA658665811
Gene: ST14 HGNC NCBI

Linked Data

ClinVar Variation Id: 452396
ClinVar RCV Id: RCV000520395
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068813.1:p.Pro298His
CA6363799
NM_021978.4:c.893C>A