Canonical Allele Identifier: PA239074
Gene: FREM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 193530
ClinVar RCV Id: RCV000293781 RCV000724593 RCV001818413 RCV003955015
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997244.4:p.Ser527Leu
CA239073
NM_207361.6:c.1580C>T