Canonical Allele Identifier: PA2826462932
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 220157
ClinVar RCV Id: RCV000204442 RCV000214137 RCV000759837 RCV002485345 RCV003320603 RCV003315420 RCV003997618
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gln104Glu
CA039073
NM_001258281.1:c.310C>G