Canonical Allele Identifier: PA645418482
Gene: FREM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 366124
ClinVar RCV Id: RCV000332215 RCV000953604
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659403.4:p.Thr1415Ser
CA4990243
NM_144966.7:c.4244C>G
CA372966314
NM_144966.7:c.4243A>T