Canonical Allele Identifier: PA2826050238
Gene: FHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2109292
ClinVar RCV Id: RCV003038283
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161291.1:p.Val237Met
CA414609630
NM_001167819.1:c.709G>A