Canonical Allele Identifier: PA2742023425
Gene: SLC51B HGNC NCBI
ClinVar RCV:
RCV003705340
ClinVar Variation:
2869132
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_849190.2:p.Val16Ile
CA392870813
NM_178859.4:c.46G>A