Canonical Allele Identifier: PA211671
Gene: MSH2 HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Pro349Ala
CA016975
NM_000251.3:c.1045C>G
CA3273124182
NM_000251.3:c.1045_1047delinsGCG
CA3273124184
NM_000251.3:c.1045_1047delinsGCC
CA3273124186
NM_000251.3:c.1045_1047delinsGCA