Canonical Allele Identifier: PA2579912408
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3074155
ClinVar RCV Id: RCV004012697
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gln218Arg
CA346731675
NM_000251.3:c.653A>G