Canonical Allele Identifier: PA1139674588
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 925462
ClinVar RCV Id: RCV001187429

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys1416Glu
CA041397
NM_000257.4:c.4246A>G