Canonical Allele Identifier: PA645382985
Gene: FH HGNC NCBI
ClinVar RCV:
RCV000445594
ClinVar Variation:
393573
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Ala274Pro
CA16609367
NM_000143.4:c.820G>C