Canonical Allele Identifier: PA2826630986
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 820409
ClinVar RCV Id: RCV001013833 RCV003492203
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Gly350Ala
CA346750574
NM_001281493.2:c.1049G>C