Canonical Allele Identifier: PA2573099383
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1326433

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Thr300Ala
CA391933499
NM_152594.3:c.898A>G