Canonical Allele Identifier: PA2826465471
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1789912
ClinVar RCV Id: RCV002428528 RCV003098815 RCV004007423 RCV004526930
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Thr716Ala
CA46705083
NM_001258281.1:c.2146A>G