Canonical Allele Identifier: PA2742014994
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2997217
ClinVar RCV Id: RCV003851336
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Thr7Ile
CA391931835
NM_152594.3:c.20C>T