Canonical Allele Identifier: PA2741810059
Gene: F11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2734694
ClinVar RCV Id: RCV003555169

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000119.1:p.Gly368Arg
CA358938933
NM_000128.4:c.1102G>A
CA358938934
NM_000128.4:c.1102G>C