Canonical Allele Identifier: PA2826032823
Gene: SLC16A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2831753
ClinVar RCV Id: RCV003686764

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159968.1:p.Glu241Asp
CA341828357
NM_001166496.2:c.723G>C
CA341828358
NM_001166496.2:c.723G>T