Canonical Allele Identifier: PA2826636020
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 525805
ClinVar RCV Id: RCV000630124
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Pro466Arg
CA46710789
NM_001281494.2:c.1397C>G