Canonical Allele Identifier: PA915985915
Gene: FHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 222635
ClinVar RCV Id: RCV000208197 RCV000263325 RCV000822468 RCV004020556
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153173.1:p.Cys284Ser
CA351843
NM_001159701.2:c.851G>C
CA414609784
NM_001159701.2:c.850T>A