Canonical Allele Identifier: PA1139756502
Gene: FREM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 914685
ClinVar RCV Id: RCV001168978 RCV004032910
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659403.4:p.Thr1413Arg
CA4990247
NM_144966.7:c.4238C>G