Canonical Allele Identifier: PA2579919382
Gene: MSH2 HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Leu634Phe
CA346728598
NM_000251.3:c.1902A>C
CA346728599
NM_000251.3:c.1902A>T