Canonical Allele Identifier: PA2826465179
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 455544
ClinVar RCV Id: RCV000546593
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Val639Leu
CA346729255
NM_001258281.1:c.1915G>T
CA346729256
NM_001258281.1:c.1915G>C