Canonical Allele Identifier: PA645471207
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 246289
ClinVar RCV Id: RCV000236172 RCV000630120 RCV003298310
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly62Ala
CA10584202
NM_000251.3:c.185G>C