Canonical Allele Identifier: PA645502397
Gene: FREM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 311987
ClinVar RCV Id: RCV000399182 RCV002056381 RCV004021573
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997244.4:p.Ala1664Thr
CA6955112
NM_207361.6:c.4990G>A