Canonical Allele Identifier: PA2825112095
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2088164
ClinVar RCV Id: RCV003018034

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Leu978Pro
CA389046501
NM_000257.4:c.2933T>C