Canonical Allele Identifier: PA1139674728
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 924360
ClinVar RCV Id: RCV001185648 RCV003462659
ClinVar Variation Id: 2701756
ClinVar RCV Id: RCV003594924 RCV004366487
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gly752Ser
CA346752701
NM_000179.3:c.2254G>A
CA2697548118
NM_000179.3:c.2253_2254delinsCA