Canonical Allele Identifier: PA645475510
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 230720
ClinVar RCV Id: RCV000213595 RCV002518276 RCV003997857
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Leu736Phe
CA10578000
NM_000251.3:c.2206C>T