Canonical Allele Identifier: PA645430388
Gene: SPART HGNC NCBI

Linked Data

ClinVar Variation Id: 311767

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055902.1:p.Ala472Ser
CA6949398
NM_015087.5:c.1414G>T