Canonical Allele Identifier: PA2830318377
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3229264
ClinVar RCV Id: RCV004524843
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Arg341Ser
CA391933816
NM_152594.3:c.1023G>C
CA391933817
NM_152594.3:c.1023G>T