Canonical Allele Identifier: PA2826465676
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 231967
ClinVar RCV Id: RCV000218052 RCV000629882 RCV001175264 RCV003997937
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.His773Asp
CA10578009
NM_001258281.1:c.2317C>G