Allele Registry

Canonical Allele Identifier: PA126638

Gene: F13A1 HGNC NCBI

ClinVar RCV:

RCV000017996

RCV000017997

RCV000248039

RCV000374698

RCV000998517

ClinVar Variation:

16532

HGVS (amino-acid)	Matching Registered Transcripts
NP_000120.2:p.Val35Leu	CA126636 NM_000129.4:c.103G>T CA362740542 NM_000129.4:c.103G>C