Canonical Allele Identifier: PA2579922216
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2826185
ClinVar RCV Id: RCV003761091
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Val802Ala
CA346730200
NM_000251.3:c.2405T>C