Canonical Allele Identifier: PA2573162565
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 1432248
ClinVar RCV Id: RCV002560740 RCV004042049
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Phe50Leu
CA345442010
NM_000143.4:c.150C>G
CA345442011
NM_000143.4:c.150C>A
CA345442019
NM_000143.4:c.148T>C