Canonical Allele Identifier: PA658672220
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 449782
ClinVar RCV Id: RCV000519754 RCV001010007 RCV000547472
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Pro385Ala
CA46702663
NM_000251.3:c.1153C>G