Canonical Allele Identifier: PA645426870
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 415718
ClinVar RCV Id: RCV000466135 RCV001260393 RCV001813484 RCV001637045 RCV004022975
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Asn10Lys
CA7469949
NM_152594.3:c.30C>A
CA391931853
NM_152594.3:c.30C>G