Canonical Allele Identifier: PA2742023427
Gene: SLC51B HGNC NCBI

Linked Data

ClinVar Variation Id: 2785008
ClinVar RCV Id: RCV003662590
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_849190.2:p.Glu23Asp
CA392871098
NM_178859.4:c.69G>C
CA392871099
NM_178859.4:c.69G>T