Canonical Allele Identifier: PA164307
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 141042

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Glu852Asp
CA020728
NM_000251.3:c.2556G>C
CA346730899
NM_000251.3:c.2556G>T