Canonical Allele Identifier: PA645383401
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 405910
ClinVar RCV Id: RCV002523293
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Pro503_Lys504dup
CA16610022
NM_000143.4:c.1508_1509insCAAACC