Canonical Allele Identifier: PA2499232975
Gene: F2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1098519
ClinVar RCV Id: RCV001420453
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000497.1:p.Gly332Ala
CA380267082
NM_000506.5:c.995G>C