Canonical Allele Identifier: PA2826465015
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90855
ClinVar RCV Id: RCV000220086 RCV000483333 RCV000524371 RCV000765672 RCV002265597 RCV003389040 RCV003997156
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Pro604Leu
CA019790
NM_001258281.1:c.1811C>T