Canonical Allele Identifier: PA2741882062
Gene: MTAP HGNC NCBI

Linked Data

ClinVar Variation Id: 2659127
ClinVar RCV Id: RCV003425638

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001382969.1:p.Asn69Asp
CA373084935
NM_001396040.1:c.205A>G