ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2828618419
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_001362484.1:p.Ala594Ser
CA2081902
NM_001375555.1:c.1780G>T