Canonical Allele Identifier: PA2828317741
Gene: FHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2797468
ClinVar RCV Id: RCV003624785
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356257.1:p.Thr315Ser
CA414609728
NM_001369328.1:c.943A>T
CA414609732
NM_001369328.1:c.944C>G