Canonical Allele Identifier: PA2580503729
Gene: NRSN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2384861
ClinVar RCV Id: RCV004217678

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542454.3:p.Val99Leu
CA363276745
NM_080723.5:c.295G>C
CA363276746
NM_080723.5:c.295G>T