Canonical Allele Identifier: PA658735871
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 489911
ClinVar RCV Id: RCV000580341 RCV001037648
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Phe37Leu
CA346728788
NM_000251.3:c.109T>C
CA346728799
NM_000251.3:c.111C>A
CA346728801
NM_000251.3:c.111C>G