Canonical Allele Identifier: PA645417106
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 235033

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu1468Lys
CA10581170
NM_000257.4:c.4402G>A