Canonical Allele Identifier: PA645502390
Gene: FREM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 311979
ClinVar RCV Id: RCV000376652 RCV000928533 RCV001252825
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997244.4:p.Pro1553Ala
CA6955045
NM_207361.6:c.4657C>G