Canonical Allele Identifier: PA1139677336
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 919342

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala230Asp
CA346731907
NM_000251.3:c.689C>A