Canonical Allele Identifier: PA645474372
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 246481
ClinVar RCV Id: RCV000236460 RCV001047851 RCV003165662 RCV003998929
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Met492Leu
CA028758
NM_000251.3:c.1474A>T
CA346727068
NM_000251.3:c.1474A>C