Canonical Allele Identifier: PA2580107037
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 1768391
ClinVar RCV Id: RCV002387299
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Met328Ile
CA345438282
NM_000143.4:c.984G>A
CA345438283
NM_000143.4:c.984G>C
CA345438284
NM_000143.4:c.984G>T