Canonical Allele Identifier: PA2826922908
Gene: SNCAIP HGNC NCBI

Linked Data

ClinVar Variation Id: 2246460
ClinVar RCV Id: RCV004104402
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295037.1:p.Met414Leu
CA360883761
NM_001308108.1:c.1240A>C
CA360883762
NM_001308108.1:c.1240A>T