Canonical Allele Identifier: PA2579911099
Gene: MSH2 HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Met141Ile
CA346730442
NM_000251.3:c.423G>A
CA346730443
NM_000251.3:c.423G>C
CA346730444
NM_000251.3:c.423G>T