Canonical Allele Identifier: PA915985811
Gene: FHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 646065
ClinVar RCV Id: RCV000800282
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153173.1:p.Phe156Leu
CA414608390
NM_001159701.2:c.466T>C
CA414608395
NM_001159701.2:c.468C>A
CA414608396
NM_001159701.2:c.468C>G