Canonical Allele Identifier: PA2580104948
Gene: F13A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2429375
ClinVar RCV Id: RCV003126312
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000120.2:p.Gly313Arg
CA362739933
NM_000129.4:c.937G>C