Canonical Allele Identifier: PA2826465092
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90875
ClinVar RCV Id: RCV000165796 RCV000410248 RCV000524376 RCV001030713 RCV001260344 RCV001588898 RCV003997157
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Met622Ile
CA019942
NM_001258281.1:c.1866G>A
CA346729170
NM_001258281.1:c.1866G>C
CA346729171
NM_001258281.1:c.1866G>T