Canonical Allele Identifier: PA2826313342
Gene: SNCAIP HGNC NCBI

Linked Data

ClinVar Variation Id: 2246460
ClinVar RCV Id: RCV004104402
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229864.1:p.Met354Leu
CA360883761
NM_001242935.3:c.1060A>C
CA360883762
NM_001242935.3:c.1060A>T