Canonical Allele Identifier: PA2742023434
Gene: SLC51B HGNC NCBI

Linked Data

ClinVar Variation Id: 3061220
ClinVar RCV Id: RCV003982732
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_849190.2:p.Val77Ala
CA392842463
NM_178859.4:c.230T>C