Canonical Allele Identifier: PA2826464478
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 134842
ClinVar RCV Id: RCV000121560 RCV000472209 RCV000569681 RCV001588967 RCV003460853
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile478Thr
CA018761
NM_001258281.1:c.1433T>C