Canonical Allele Identifier: PA2579923713
Gene: MSH2 HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Val891Leu
CA346731485
NM_000251.3:c.2671G>T
CA346731487
NM_000251.3:c.2671G>C