Canonical Allele Identifier: PA645498206
Gene: SLC27A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 289551
ClinVar RCV Id: RCV000404832 RCV003977808
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036386.1:p.Val312Ile
CA9718148
NM_012254.3:c.934G>A