Canonical Allele Identifier: PA1139675055
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 922812
ClinVar RCV Id: RCV001183107

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu1582Asp
CA389037722
NM_000257.4:c.4746G>T
CA389037723
NM_000257.4:c.4746G>C