Canonical Allele Identifier: PA915985661
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 557209
ClinVar RCV Id: RCV000673318
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001458.1:p.Met311Val
CA229597135
NM_001467.6:c.931A>G