Canonical Allele Identifier: PA2580448671
Gene: MYH14 HGNC NCBI
ClinVar RCV:
RCV003054273
ClinVar Variation:
2122880
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079005.3:p.Gly39Arg
CA309565385
NM_024729.4:c.115G>A
CA406945806
NM_024729.4:c.115G>C