Canonical Allele Identifier: PA1139673697
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 915535
ClinVar RCV Id: RCV001170268

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1006Thr
CA389045889
NM_000257.4:c.3016G>A