Canonical Allele Identifier: PA2826465544
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 428545
ClinVar RCV Id: RCV000490997 RCV003449375
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.His735Pro
CA346730191
NM_001258281.1:c.2204A>C