Canonical Allele Identifier: PA354622
Gene: FREM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 218843
ClinVar RCV Id: RCV000202844 RCV001168977 RCV001331739 RCV002478723 RCV004020500 RCV002515510
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659403.4:p.Ser1471Asn
CA249047
NM_144966.7:c.4412G>A