Allele Registry

Canonical Allele Identifier: PA1139705496

Gene: SLC37A4 HGNC NCBI

ClinVar RCV:

RCV000007342

ClinVar Variation:

6930

HGVS (amino-acid)	Matching Registered Transcripts
NP_001458.1:p.Val236del	CA254002 NM_001467.6:c.706_708del