Canonical Allele Identifier: PA2573062009
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1317240
ClinVar RCV Id: RCV001759112

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1126Leu
CA389044084
NM_000257.4:c.3377G>T