Canonical Allele Identifier: PA2826464739
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 216344
ClinVar RCV Id: RCV000199035 RCV000235488 RCV000412070 RCV000566201 RCV003323451 RCV003997014
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Val539Phe
CA031537
NM_001258281.1:c.1615G>T