Canonical Allele Identifier: PA2580544487
Gene: SLC51B HGNC NCBI
ClinVar RCV:
RCV003085672
ClinVar Variation:
2153457
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_849190.2:p.Val15Leu
CA271519348
NM_178859.4:c.43G>T
CA392870758
NM_178859.4:c.43G>C