Canonical Allele Identifier: PA2825841132
Gene: SPART HGNC NCBI

Linked Data

ClinVar Variation Id: 311767

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135767.1:p.Ala472Ser
CA6949398
NM_001142295.2:c.1414G>T