Canonical Allele Identifier: PA2826635528
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2587354
ClinVar RCV Id: RCV003360828
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Leu353Phe
CA346750590
NM_001281494.2:c.1059A>C
CA346750591
NM_001281494.2:c.1059A>T