Canonical Allele Identifier: PA1139680293
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 927535
ClinVar RCV Id: RCV001190855
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Met663Leu
CA032288
NM_000251.3:c.1987A>T
CA346728896
NM_000251.3:c.1987A>C