Canonical Allele Identifier: PA915957989
Gene: F11 HGNC NCBI

Linked Data

ClinVar Variation Id: 627105
ClinVar RCV Id: RCV000851837
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000119.1:p.Asp212Asn
CA358959094
NM_000128.4:c.634G>A