Allele Registry

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Canonical Allele Identifier: PA2580338838

Gene: SLC19A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2229943

ClinVar RCV Id: RCV002712688

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_008927.1:p.Thr65Ser	CA343112088 NM_006996.3:c.194C>G CA343112090 NM_006996.3:c.193A>T