Canonical Allele Identifier: PA2826464795
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 142665
ClinVar RCV Id: RCV000132012 RCV000629677 RCV001030712 RCV003129784 RCV003998127
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Pro550Ser
CA019428
NM_001258281.1:c.1648C>T