Canonical Allele Identifier: PA913201482
Gene: FHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 537357
ClinVar RCV Id: RCV000646188
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153171.1:p.Cys292Ser
CA414609924
NM_001159699.2:c.874T>A
CA414609929
NM_001159699.2:c.875G>C