Canonical Allele Identifier: PA1139705547
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 971103
ClinVar RCV Id: RCV001246799
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001458.1:p.Tyr296Gln
CA1139662377
NM_001467.6:c.886_888delinsCAA