Canonical Allele Identifier: PA2826464278
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 455498
ClinVar RCV Id: RCV000553969 RCV003159731 RCV003459176
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Met426Ile
CA346727075
NM_001258281.1:c.1278G>A
CA346727077
NM_001258281.1:c.1278G>C
CA346727079
NM_001258281.1:c.1278G>T