Canonical Allele Identifier: PA2580269702
Gene: MSH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1771808
ClinVar RCV Id: RCV002389285 RCV003120997
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002430.3:p.Asn345Tyr
CA360267832
NM_002439.5:c.1033A>T