Canonical Allele Identifier: PA2741810089
Gene: F11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2893640
ClinVar RCV Id: RCV003732919
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000119.1:p.Thr593Ser
CA358946061
NM_000128.4:c.1777A>T