Canonical Allele Identifier: PA121873
Gene: F7 HGNC NCBI

Linked Data

ClinVar Variation Id: 12088
ClinVar RCV Id: RCV000012869
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_062562.1:p.His386Gln
CA121870
NM_019616.4:c.1158T>G
CA388786802
NM_019616.4:c.1158T>A