Canonical Allele Identifier: PA645294465
Gene: F5 HGNC NCBI

Linked Data

ClinVar Variation Id: 293621
ClinVar RCV Id: RCV000260117 RCV000319985 RCV000332909 RCV000373517 RCV002429244 RCV002292439 RCV003761906 RCV003930208
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000121.2:p.Asn741Ser
CA1234128
NM_000130.5:c.2222A>G