Canonical Allele Identifier: PA2827036852
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_001306596.1:p.Thr65Ser
CA343112088
NM_001319667.1:c.194C>G
CA343112090
NM_001319667.1:c.193A>T