Canonical Allele Identifier: PA645294535
Gene: F13A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 255183
ClinVar RCV Id: RCV000242868 RCV000366204 RCV000998515
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000120.2:p.Pro565Leu
CA3624279
NM_000129.4:c.1694C>T