Canonical Allele Identifier: PA1139733736
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 993637
ClinVar RCV Id: RCV001285320 RCV003399053 RCV003987825
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_063916.1:p.Tyr40del
CA1139667895
NM_019863.3:c.118_120del