Canonical Allele Identifier: PA2826472841
Gene: SMS HGNC NCBI

Linked Data

ClinVar Variation Id: 2500736
ClinVar RCV Id: RCV003225648

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245352.1:p.Val172Ala
CA412568994
NM_001258423.2:c.515T>C