Canonical Allele Identifier: PA2580520957
Gene: FREM1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659403.4:p.Asp922Asn
CA4990821
NM_144966.7:c.2764G>A