Canonical Allele Identifier: PA1139678305
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 985649
ClinVar RCV Id: RCV001266670
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Tyr68His
CA345441843
NM_000143.4:c.202T>C