Canonical Allele Identifier: PA1139678287
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 957362
ClinVar RCV Id: RCV001230326
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Lys61Gln
CA345441912
NM_000143.4:c.181A>C