Canonical Allele Identifier: PA645502379
Gene: FREM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 311970
ClinVar RCV Id: RCV003765821 RCV000369260
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997244.4:p.Met1328Thr
CA6954894
NM_207361.6:c.3983T>C