Canonical Allele Identifier: PA2580521000
Gene: FREM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2281029
ClinVar RCV Id: RCV002823265

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659403.4:p.Val1404Leu
CA372966381
NM_144966.7:c.4210G>T
CA372966383
NM_144966.7:c.4210G>C