Canonical Allele Identifier: PA645426967
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 280174
ClinVar RCV Id: RCV000343889 RCV001238249 RCV004021063
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Asn269Lys
CA10603437
NM_152594.3:c.807T>G
CA391933293
NM_152594.3:c.807T>A