Canonical Allele Identifier: PA645474247
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408511
ClinVar RCV Id: RCV000473948 RCV000780437 RCV000774562 RCV004000786
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Pro415Ser
CA16610806
NM_000251.3:c.1243C>T