Canonical Allele Identifier: PA159742
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 41583
ClinVar RCV Id: RCV000034485 RCV000121091 RCV000166620 RCV000687788
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Ala295Thr
CA159740
NM_000143.4:c.883G>A