Canonical Allele Identifier: PA2742015152
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2627335
ClinVar RCV Id: RCV003388529 RCV003600459
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Asp270Tyr
CA391933295
NM_152594.3:c.808G>T