Canonical Allele Identifier: PA2580195214
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_001295029.1:p.Met767Leu
CA360883761
NM_001308100.2:c.2299A>C
CA360883762
NM_001308100.2:c.2299A>T