Canonical Allele Identifier: PA1139678611
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 958929
ClinVar RCV Id: RCV002348780 RCV002563775
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Gly166Arg
CA345439971
NM_000143.4:c.496G>A
CA345439972
NM_000143.4:c.496G>C