Canonical Allele Identifier: PA2826629355
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 188188
ClinVar RCV Id: RCV000168100 RCV000213342 RCV000663216 RCV001800508 RCV003462256 RCV003987391 RCV003995607
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu1205Asp
CA015307
NM_001281492.2:c.3615A>C
CA346761626
NM_001281492.2:c.3615A>T