Canonical Allele Identifier: PA2741925920
Gene: MAP1B HGNC NCBI
ClinVar RCV:
RCV003448826
ClinVar Variation:
2671742
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005900.2:p.Thr603Asn
CA3298742
NM_005909.5:c.1808C>A