Canonical Allele Identifier: PA216370
Gene: GCM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 64542
ClinVar RCV Id: RCV000054729

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004743.1:p.Ala278Val
CA216369
NM_004752.4:c.833C>T