Canonical Allele Identifier: PA2827331222
Gene: SCP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 523456
ClinVar RCV Id: RCV003444609

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317516.1:p.Gly67Ser
CA340386325
NM_001330587.2:c.199G>A