Canonical Allele Identifier: PA645378946
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 419819
ClinVar Variation Id: 950784
ClinVar RCV Id: RCV001222570

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Val263Leu
CA16617635
NM_000179.3:c.787G>C
CA346740274
NM_000179.3:c.787G>T