Canonical Allele Identifier: PA2828317349
Gene: FHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2736335
ClinVar RCV Id: RCV003513638
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356256.1:p.Cys126Ser
CA414608381
NM_001369327.2:c.376T>A
CA414608385
NM_001369327.2:c.377G>C