Canonical Allele Identifier: PA2499298962
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1061139
ClinVar RCV Id: RCV001370671 RCV001786479
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Cys368Ser
CA391934137
NM_152594.3:c.1102T>A
CA391934144
NM_152594.3:c.1103G>C