Canonical Allele Identifier: PA126641
Gene: F13A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16533
ClinVar RCV Id: RCV000017998 RCV003325450
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000120.2:p.Arg327Gln
CA126639
NM_000129.4:c.980G>A