Canonical Allele Identifier: PA2579912701
Gene: MSH2 HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Lys235Asn
CA346732020
NM_000251.3:c.705A>C
CA346732023
NM_000251.3:c.705A>T