Canonical Allele Identifier: PA2741899855
Gene: SCG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2610941
ClinVar RCV Id: RCV004351703

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003460.2:p.Asn407Ser
CA2138008
NM_003469.5:c.1220A>G