Canonical Allele Identifier: PA2741929089
Gene: SLC16A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2632344
ClinVar RCV Id: RCV003416768

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006508.2:p.Glu54Asp
CA413655907
NM_006517.5:c.162G>C
CA413655908
NM_006517.5:c.162G>T