Canonical Allele Identifier: PA2742015151
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2721394
ClinVar RCV Id: RCV003499520
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Met266Ile
CA391933267
NM_152594.3:c.798G>T
CA391933268
NM_152594.3:c.798G>C
CA391933269
NM_152594.3:c.798G>A