Canonical Allele Identifier: PA103464
Gene: F7 HGNC NCBI

Linked Data

ClinVar Variation Id: 374352
ClinVar RCV Id: RCV000415275 RCV003950324
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000122.1:p.Ala429Thr
CA7060252
NM_000131.4:c.1285G>A