Canonical Allele Identifier: PA121853
Gene: F7 HGNC NCBI

Linked Data

ClinVar Variation Id: 12076
ClinVar RCV Id: RCV000012857 RCV000851974 RCV002243638 RCV002496330 RCV001091742
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_062562.1:p.Ala332Val
CA121850
NM_019616.4:c.995C>T