Canonical Allele Identifier: PA2827036801
Gene: SLC19A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2615475
ClinVar RCV Id: RCV003367445

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001306596.1:p.Asp2Glu
CA343112671
NM_001319667.1:c.6T>G
CA343112673
NM_001319667.1:c.6T>A