Canonical Allele Identifier: PA2573304214
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1371770
ClinVar RCV Id: RCV001899658

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Ser303Arg
CA391933518
NM_152594.3:c.907A>C
CA391933524
NM_152594.3:c.909T>G
CA391933525
NM_152594.3:c.909T>A