Canonical Allele Identifier: PA1139678764
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 855318
ClinVar RCV Id: RCV002255615 RCV002553885
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.His215Leu
CA345439326
NM_000143.4:c.644A>T