Canonical Allele Identifier: PA915988190
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 552538
ClinVar RCV Id: RCV000667820
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157751.1:p.Phe61Leu
CA382903967
NM_001164279.2:c.183T>G
CA382903974
NM_001164279.2:c.183T>A
CA382903995
NM_001164279.2:c.181T>C