Canonical Allele Identifier: PA645441078
Gene: SNCAIP HGNC NCBI

Linked Data

ClinVar Variation Id: 350498
ClinVar RCV Id: RCV000298051 RCV000455101 RCV000971881
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005451.2:p.Glu709Gln
CA3385033
NM_005460.4:c.2125G>C