Canonical Allele Identifier: PA2828617056
Gene: MAP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 252604
ClinVar RCV Id: RCV000239245

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362463.1:p.Ala752Ser
CA2081902
NM_001375534.1:c.2254G>T