Canonical Allele Identifier: PA2825934611
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_001153175.1:p.Thr186Ser
CA414609728
NM_001159703.2:c.556A>T
CA414609732
NM_001159703.2:c.557C>G