Canonical Allele Identifier: PA2827246270
Gene: MAP1B HGNC NCBI
ClinVar RCV:
RCV003448826
ClinVar Variation:
2671742
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311184.1:p.Thr477Asn
CA3298742
NM_001324255.2:c.1430C>A