Canonical Allele Identifier: PA658680191
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 485557
ClinVar RCV Id: RCV000565315 RCV001273185 RCV002528977
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Ile52Leu
CA1478757
NM_000143.4:c.154A>T
CA345442004
NM_000143.4:c.154A>C