Canonical Allele Identifier: PA2826465912
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 655967
ClinVar RCV Id: RCV000812256 RCV004028764
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Pro829Ser
CA346731551
NM_001258281.1:c.2485C>T