Canonical Allele Identifier: PA2826631375
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 3230528
ClinVar RCV Id: RCV004520679
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Asn440Asp
CA346752456
NM_001281493.2:c.1318A>G