Canonical Allele Identifier: PA645294448
Gene: F5 HGNC NCBI

Linked Data

ClinVar Variation Id: 293639
ClinVar RCV Id: RCV000276953 RCV000317190 RCV000353339 RCV000386447 RCV000521560 RCV003595930
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000121.2:p.His175Arg
CA1234592
NM_000130.5:c.524A>G