Canonical Allele Identifier: PA103198
Gene: F11 HGNC NCBI

Linked Data

ClinVar Variation Id: 11900
ClinVar RCV Id: RCV000012675

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000119.1:p.Ser594Arg
CA121761
NM_000128.4:c.1782C>A
CA358946072
NM_000128.4:c.1780A>C
CA358946080
NM_000128.4:c.1782C>G