Canonical Allele Identifier: PA658825429
Gene: F11 HGNC NCBI

Linked Data

ClinVar Variation Id: 551022
ClinVar RCV Id: RCV000665972 RCV003227822
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000119.1:p.Arg268His
CA3163786
NM_000128.4:c.803G>A