Canonical Allele Identifier: PA121878
Gene: F7 HGNC NCBI

Linked Data

ClinVar Variation Id: 12090
ClinVar RCV Id: RCV000012871
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000122.1:p.Phe328Ser
CA121874
NM_000131.4:c.983T>C