Canonical Allele Identifier: PA095060
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 629222
ClinVar RCV Id: RCV000773921 RCV000819683
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Met729Val
CA346729391
NM_000251.3:c.2185A>G