Canonical Allele Identifier: PA1139675151
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 845585
ClinVar RCV Id: RCV001048683
ClinVar Variation Id: 1039123

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gln1647His
CA044255
NM_000257.4:c.4941G>C
CA389037303
NM_000257.4:c.4941G>T