Canonical Allele Identifier: PA2828618517
Gene: MAP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 252604
ClinVar RCV Id: RCV000239245

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362485.1:p.Ala594Ser
CA2081902
NM_001375556.1:c.1780G>T