Canonical Allele Identifier: PA2580305327
Gene: SMS HGNC NCBI

Linked Data

ClinVar Variation Id: 2500736
ClinVar RCV Id: RCV003225648
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004586.2:p.Val225Ala
CA412568994
NM_004595.5:c.674T>C