Canonical Allele Identifier: PA645294462
Gene: F5 HGNC NCBI

Linked Data

ClinVar Variation Id: 293623
ClinVar RCV Id: RCV000310778 RCV000314115 RCV000371161 RCV000400024
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000121.2:p.Asp681Gly
CA10608720
NM_000130.5:c.2042A>G