Canonical Allele Identifier: PA2573304203
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1360401
ClinVar RCV Id: RCV001864941 RCV002361104
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Gln215His
CA269293278
NM_152594.3:c.645A>C
CA391932904
NM_152594.3:c.645A>T