Canonical Allele Identifier: PA645447835
Gene: MAP6 HGNC NCBI

Linked Data

ClinVar Variation Id: 252761
ClinVar RCV Id: RCV000238957
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_149052.1:p.Arg740His
CA6191106
NM_033063.2:c.2219G>A