Canonical Allele Identifier: PA1139675133
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 920998
ClinVar RCV Id: RCV001180138

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gln1640Pro
CA389037356
NM_000257.4:c.4919A>C