Canonical Allele Identifier: PA104091
Gene: F7 HGNC NCBI

Linked Data

ClinVar Variation Id: 12088
ClinVar RCV Id: RCV000012869
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000122.1:p.His408Gln
CA121870
NM_000131.4:c.1224T>G
CA388786802
NM_000131.4:c.1224T>A