Canonical Allele Identifier: PA2741812922
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 2908203
ClinVar RCV Id: RCV003729657
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Ala128Val
CA345440224
NM_000143.4:c.383C>T