Canonical Allele Identifier: PA2580282039
Gene: SCG2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003460.2:p.Gln557Leu
CA2137936
NM_003469.5:c.1670A>T