Canonical Allele Identifier: PA2829335330
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2084912
ClinVar RCV Id: RCV003011384

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001458.1:p.Asn374Ser
CA382895049
NM_001467.6:c.1121A>G