Canonical Allele Identifier: PA2827246435
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_001311184.1:p.Gly1729Arg
CA360019027
NM_001324255.2:c.5185G>C