Canonical Allele Identifier: PA2828374116
Gene: FREM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 913237
ClinVar RCV Id: RCV001166769 RCV002483928 RCV002558635
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356994.1:p.Leu182Val
CA372963765
NM_001370065.1:c.544C>G