Canonical Allele Identifier: PA645502429
Gene: FREM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 312019
ClinVar RCV Id: RCV000380191 RCV001089662 RCV002056385 RCV003910166
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997244.4:p.Val2555Leu
CA6955953
NM_207361.6:c.7663G>T
CA387899777
NM_207361.6:c.7663G>C