Canonical Allele Identifier: PA2828807164
Gene: FREM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 218843
ClinVar RCV Id: RCV000202844 RCV001168977 RCV001331739 RCV002478723 RCV004020500 RCV002515510
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366010.1:p.Ser1471Asn
CA249047
NM_001379081.2:c.4412G>A