Canonical Allele Identifier: PA2826625727
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1769757
ClinVar RCV Id: RCV002385540
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Met308Ile
CA346744388
NM_001281492.2:c.924G>A
CA346744389
NM_001281492.2:c.924G>C
CA346744390
NM_001281492.2:c.924G>T