Canonical Allele Identifier: PA1139678284
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 960737
ClinVar RCV Id: RCV002563812
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Lys61Asn
CA1478753
NM_000143.4:c.183G>T
CA345441906
NM_000143.4:c.183G>C