Canonical Allele Identifier: PA645382481
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 296878
ClinVar RCV Id: RCV000307949 RCV000369616 RCV002522126 RCV002418146
ClinVar Variation Id: 641546
ClinVar RCV Id: RCV000794812 RCV002422699 RCV002535910
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Met1Leu