Canonical Allele Identifier: PA1139671776
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 942795
ClinVar RCV Id: RCV001212852

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ser241Pro
CA389052188
NM_000257.4:c.721T>C