Canonical Allele Identifier: PA2828127879
Gene: MAP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 252604
ClinVar RCV Id: RCV000239245
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350839.1:p.Ala748Ser
CA2081902
NM_001363910.2:c.2242G>T