Canonical Allele Identifier: PA1139674451
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 915736
ClinVar RCV Id: RCV001170996

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1396Leu
CA389040574
NM_000257.4:c.4187G>T