Canonical Allele Identifier: PA2829284058
Gene: MTAP HGNC NCBI

Linked Data

ClinVar Variation Id: 2659127
ClinVar RCV Id: RCV003425638
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001382972.1:p.Asn52Asp
CA373084935
NM_001396043.1:c.154A>G