Canonical Allele Identifier: PA2825113427
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2766678
ClinVar RCV Id: RCV003587980

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Met1764Ile
CA389035944
NM_000257.4:c.5292G>T
CA389035946
NM_000257.4:c.5292G>C
CA389035948
NM_000257.4:c.5292G>A