Canonical Allele Identifier: PA357879
Gene: FREM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 218939
ClinVar RCV Id: RCV000203291 RCV000289080 RCV000249912 RCV002057046
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659403.4:p.Gly465Ala
CA339661
NM_144966.7:c.1394G>C