Canonical Allele Identifier: PA2828317101
Gene: FHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1058447
ClinVar RCV Id: RCV001367591 RCV003145628
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356255.1:p.Thr152Ser
CA414608567
NM_001369326.1:c.454A>T
CA414608569
NM_001369326.1:c.455C>G