Canonical Allele Identifier: PA1139673768
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 934193
ClinVar RCV Id: RCV001202536

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gly1036_Glu1039del
CA1139663386
NM_000257.4:c.3105_3116del