Canonical Allele Identifier: PA2829587098
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_005451.2:p.Ser716Arg
CA125942626
NM_005460.4:c.2148C>G
CA360883731
NM_005460.4:c.2146A>C
CA360883739
NM_005460.4:c.2148C>A