Canonical Allele Identifier: PA645502358
Gene: FREM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 311953
ClinVar RCV Id: RCV000401773 RCV000873153
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997244.4:p.Arg688Gly
CA6954528
NM_207361.6:c.2062C>G