Canonical Allele Identifier: PA2826465530
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 525747
ClinVar RCV Id: RCV000630005 RCV001015381 RCV004002788
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asn732Thr
CA346730165
NM_001258281.1:c.2195A>C