Canonical Allele Identifier: PA108815
Gene: SLC16A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 8914

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159968.1:p.Lys204Glu
CA119996
NM_001166496.2:c.610A>G