Canonical Allele Identifier: PA2825971089
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 965824
ClinVar RCV Id: RCV001240365 RCV002379916 RCV002484315 RCV003414042
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157749.1:p.Pro43Ser
CA6311909
NM_001164277.2:c.127C>T