Canonical Allele Identifier: PA2826922961
Gene: SNCAIP HGNC NCBI

Linked Data

ClinVar Variation Id: 2275733
ClinVar RCV Id: RCV004124561
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295038.1:p.Ser312Arg
CA125942626
NM_001308109.2:c.936C>G
CA360883731
NM_001308109.2:c.934A>C
CA360883739
NM_001308109.2:c.936C>A