Canonical Allele Identifier: PA103127
Gene: F11 HGNC NCBI

Linked Data

ClinVar Variation Id: 11892
ClinVar RCV Id: RCV000012667 RCV000727626 RCV001273722 RCV001258090 RCV003407319
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000119.1:p.Phe301Leu
CA121748
NM_000128.4:c.901T>C
CA358937694
NM_000128.4:c.903C>G
CA358937696
NM_000128.4:c.903C>A