Canonical Allele Identifier: PA247858
Gene: FREM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 198939
ClinVar RCV Id: RCV000180400 RCV002500519 RCV004020169
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997244.4:p.Ala2091Val
CA247857
NM_207361.6:c.6272C>T