Canonical Allele Identifier: PA915960708
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 656363
ClinVar RCV Id: RCV002538131
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Met412Ile
CA345437209
NM_000143.4:c.1236G>A
CA345437210
NM_000143.4:c.1236G>C
CA345437212
NM_000143.4:c.1236G>T