Canonical Allele Identifier: PA2828317736
Gene: FHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3022735
ClinVar RCV Id: RCV003881921
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356257.1:p.Pro311Leu
CA414609699
NM_001369328.1:c.932C>T