Canonical Allele Identifier: PA2828806879
Gene: FREM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 218939
ClinVar RCV Id: RCV000203291 RCV000289080 RCV000249912 RCV002057046
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366010.1:p.Gly465Ala
CA339661
NM_001379081.2:c.1394G>C