Canonical Allele Identifier: PA658806840
Gene: SCP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 523456
ClinVar RCV Id: RCV003444609

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002970.2:p.Gly67Ser
CA340386325
NM_002979.5:c.199G>A