Canonical Allele Identifier: PA2580520924
Gene: FREM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2478163
ClinVar RCV Id: RCV003209179
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659403.4:p.Asp549Gly
CA372960182
NM_144966.7:c.1646A>G