Canonical Allele Identifier: PA2826500827
Gene: F7 HGNC NCBI

Linked Data

ClinVar Variation Id: 12080
ClinVar RCV Id: RCV000012861 RCV000250547 RCV000391182 RCV000396014
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254483.1:p.Arg329Gln
CA121855
NM_001267554.1:c.986G>A