Canonical Allele Identifier: PA1139671678
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 935358
ClinVar RCV Id: RCV001203929

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu179Lys
CA389052597
NM_000257.4:c.535G>A