Canonical Allele Identifier: PA2826633887
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2738992
ClinVar RCV Id: RCV003593443
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ala1000Val
CA346761434
NM_001281493.2:c.2999C>T