Canonical Allele Identifier: PA2826634881
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1774467
ClinVar RCV Id: RCV002392469
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Val206Leu
CA346746400
NM_001281494.2:c.616G>C
CA346746401
NM_001281494.2:c.616G>T