Canonical Allele Identifier: PA2825934919
Gene: FHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2441433
ClinVar RCV Id: RCV003147262
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153176.1:p.Lys279Asn
CA414609952
NM_001159704.1:c.837G>C
CA414609953
NM_001159704.1:c.837G>T