Canonical Allele Identifier: PA2828806926
Gene: FREM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1989

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366010.1:p.Arg649Trp
CA115305
NM_001379081.2:c.1945C>T