Canonical Allele Identifier: PA2580329011
Gene: MAP1B HGNC NCBI

Linked Data

ClinVar Variation Id: 2442022
ClinVar RCV Id: RCV003148343 RCV003148344
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005900.2:p.Gly1855Arg
CA360019027
NM_005909.5:c.5563G>C