Canonical Allele Identifier: PA2580456812
Gene: STN1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079204.2:p.Asp157Asn
CA5676601
NM_024928.5:c.469G>A