Canonical Allele Identifier: PA2827341102
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_001317588.1:p.Thr168Ser
CA414608567
NM_001330659.2:c.502A>T
CA414608569
NM_001330659.2:c.503C>G