Canonical Allele Identifier: PA2573161984
Gene: F11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1482231
ClinVar RCV Id: RCV002002875 RCV002280909
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000119.1:p.Gly354Arg
CA3163867
NM_000128.4:c.1060G>A
CA358938720
NM_000128.4:c.1060G>C