Canonical Allele Identifier: PA103959
Gene: F7 HGNC NCBI

Linked Data

ClinVar Variation Id: 627193
ClinVar RCV Id: RCV000851965 RCV003323715
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000122.1:p.Gly343Ser
CA388786198
NM_000131.4:c.1027G>A