Canonical Allele Identifier: PA2825111967
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2022342
ClinVar RCV Id: RCV002847699

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Thr937Ser
CA389046971
NM_000257.4:c.2810C>G
CA389046974
NM_000257.4:c.2809A>T