Canonical Allele Identifier: PA645418416
Gene: FREM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 366140
ClinVar RCV Id: RCV000373588
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659403.4:p.Val929Leu
CA4990816
NM_144966.7:c.2785G>T
CA372953608
NM_144966.7:c.2785G>C