Canonical Allele Identifier: PA2499266183
Gene: SLC28A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1267759
ClinVar RCV Id: RCV001678312
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004203.2:p.Ser75Arg
CA7542118
NM_004212.4:c.225C>A
CA392246597
NM_004212.4:c.223A>C
CA392246601
NM_004212.4:c.225C>G