Canonical Allele Identifier: PA2828806997
Gene: FREM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 366140
ClinVar RCV Id: RCV000373588
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366010.1:p.Val929Leu
CA4990816
NM_001379081.2:c.2785G>T
CA372953608
NM_001379081.2:c.2785G>C