Canonical Allele Identifier: PA915960723
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 645464
ClinVar RCV Id: RCV002538025
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Met454Ile
CA1478471
NM_000143.4:c.1362G>A
CA345436387
NM_000143.4:c.1362G>T
CA345436389
NM_000143.4:c.1362G>C