Canonical Allele Identifier: PA1139673727
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 986312
ClinVar RCV Id: RCV001267642

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gln1029Pro
CA389045664
NM_000257.4:c.3086A>C