Canonical Allele Identifier: PA1139674704
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 918880

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu1462Lys
CA389038770
NM_000257.4:c.4384G>A