Canonical Allele Identifier: PA645472116
Gene: STN1 HGNC NCBI
ClinVar RCV:
RCV000417070
ClinVar Variation:
375592
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079204.2:p.Asp157Tyr
CA5676602
NM_024928.5:c.469G>T