Canonical Allele Identifier: PA2573099382
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1334308
ClinVar RCV Id: RCV001813723

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Asp275Tyr
CA7470189
NM_152594.3:c.823G>T