Canonical Allele Identifier: PA1139669447
Gene: F11 HGNC NCBI

Linked Data

ClinVar Variation Id: 903591
ClinVar RCV Id: RCV001151015 RCV003293906
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000119.1:p.Thr407Ala
CA3163924
NM_000128.4:c.1219A>G